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* Lecturer, Tropical and Emerging Infectious Disease Division, Menzies School of Health Research and School of Environmental and Life
Sciences, Charles Darwin University, Darwin, Australia.
†Associate Professor, School of Health and Sport Sciences, University of the Sunshine Coast, Sippy Downs, Queensland, Australia.
‡Senior Research Officer, Skin Pathogens Research Laboratory, Menzies School of Health Research, Institute of Advanced Studies,
in treatment failure with recurrence of symptoms Figure 21.6 Scabeitic nodules on the scrotum.
months later.
• Generalised adenopathy and eosinophilia are
present in some cases.
DIAGNOSIS
• Due to an altered immune response in immuno- Laboratory and Special Examination Microscopic
compromised subjects, the itching is less intense identification of mites, mite parts, eggs, egg shell
or absent in these subset of patients. This occurs fragments or faecal pellets of mites from skin
also because they have physical limitations, lack of scrapings, is confirmatory for diagnosis (Fig. 21.9);
control or unawareness of the defensive scratch- however, the sensitivity of this test is less than 50%.
ing movements, as in neuropsychiatric disorders,
The diagnosis becomes difficult in patients who have
osteoarticular deformities, muscular atrophy or
other neuromuscular problems. Sometimes, it is
associated with loss of sensation and hypoesthe-
sia. These patients are highly infested with mites.
3. Nodular scabies
• Violaceous, pruritic, nodules are seen on the
glans, scrotum, thighs, buttocks and axilla
(Figs 21.6 and 21.7). Mites cannot be recovered
from these nodules.
• It is believed that this represents a form of hyper-
sensitivity reaction to mite antigens.
4. Vesicular–bullous scabies
• It is commonly seen in elderly patients and is located
on the extremities or on the trunk (Fig. 21.8).
• It clinically and histologically mimics bullous
pemphigoid.
• It may result from super infection with Staphylo-
coccus aureus, with a mechanism similar to the
development of blisters in bullous impetigo.
• This condition is mainly due to the penetration
of the mite in the dermo-epidermal junction, or
a cross-reaction with bullous pemphigoid antigen
or lytic secretions produced by the mite at the der-
moepidermal junction. Figure 21.7 Multiple nodules with eczematisation on the
5. Other minor variants: These are discussed in Table 21.1. scrotum.
severe hypersensitivity reactions that result in the examination of the patient’s skin, from the surface
development of multiple excoriations or plaques. to the superficial papillary dermis. This equipment
In this situation, a biopsy or the examination of is expensive and is available only in well-resourced
scrapings obtained from the papules–vesicles may hospitals or clinics.
be helpful. The burrows may be demonstrated in The latest test is the detection of the DNA of
these cases with the help of stains such as India ink S. scabiei from cutaneous scales based on ampli-
or gentian violet. fication by polymerase chain reaction (PCR)
Epiluminescence microscopy and high- or detection by enzyme-linked immunosorbent
resolution video dermatoscopy allow comprehensive assay.
TREATMENT The treatment options can be 2. Permethrin: This is a pyrethroid component and is a
classified according to the evidence-based approach highly efficacious topical scabicide. Five per cent per-
as follows: methrin is applied overnight once a week for 2 weeks,
over the entire body from neck downwards. Although
1. Randomised controlled trials: These are available for permethrin is the most expensive of all the topical
comparison between the effects of the following drugs: applications, it has almost no allergic side effects. The
• Ivermectin versus benzyl benzoate recommended period of contact with permethrin is
• Ivermectin versus permethrin about 8 hours. A case report of the treatment of 467
• Ivermectin versus benzyl benzoate patients in an outbreak of scabies cited that a single
• Permethrin versus crotamiton application of 5% permethrin was as effective as 1%
2. Case series: These are available for the following lindane. A second application is necessary 1 week
therapies: later only if there is clear evidence of treatment fail-
• Benzyl benzoate ure. However, Walton and colleagues (1999, 2004)
• Permethrin have demonstrated growing concerns about resis-
• Ivermectin tance to permethrin in Australia. It is often used in
• Permethrin versus lindane pregnant women, and the application time is short-
3. Case reports: These are available for the following ened to 2 hours and it is also widely used in young
therapies: children (greater than 2 months). At present, despite
• Pimecrolimus the limitations of small trials, a dearth of placebo-
• Monosulfiram controlled trials, and some conflicting information;
the first-line treatment for uncomplicated scabies
General Measures Washing bed linens and cloth- continues to be 5% permethrin.
ing is highly recommended. This can be performed 3. Lindane (γ-hexachlorcyclohexane): It is available
by machine washing at 60°C followed by heat dry- as 1% cream or lotion, and its application time is
ing. Unwashed clothes can be stored in a bag for a approximately 6 hours. It is also recommended that
minimum of 3 days as mites do not survive for more the application be repeated after 1 week. A single,
6-hour application is effective in the treatment of sca-
than a few days after isolation from human host.
bies. Although it is a cost-effective topical scabicide,
Exposing mattresses to direct sunlight can also be a it can cause severe skin irritation, allergic contact der-
useful technique. Vacuuming is also beneficial. matitis and neurological symptoms such as insomnia,
irritability, vertigo, convulsions, vomiting, diarrhoea,
Drugs Used in the Treatment of Scabies The restlessness and collapse. As a result, the use of this
major factors that determine the suitability of dif- drug has been prohibited in the European Union since
ferent scabicidal drugs for patients are the age of the 2001. It is banned in children younger than 3 years
patient, presence of pregnancy and lactative stage of due its toxicity and increasing resistance.
women, efficacy of the drugs, degree of eczematisa- 4. Crotamiton: It is widely prescribed for newborn
babies. For the treatment of scabies in children
tion and the cost involved.
between 2 months and 5 years of age, 5% perme-
1. Benzyl benzoate: The treatment of thousands of thrin was compared with 10% crotamiton cream in a
cases of scabies with topical benzyl benzoate was randomised trial. Two weeks after a single overnight
documented in Denmark during the 1930s; 10–25% treatment, 30% and 13% of children were cured with
benzyl benzoate applied in the form of a cream or permethrin and crotamiton respectively, and 4 weeks
lotion is highly efficient. Benzyl benzoate requires fre- after treatment, 89% and 60% of patients respectively,
quent applications such as twice daily for 2–3 days were cured. This indicates that crotamiton may not be
and needs to be repeated after 10 days. Benzyl ben- as efficacious as permethrin. It should be applied twice
zoate is very effective when used correctly. If not, it a day for five consecutive days, and the contact period
may cause skin irritation and or a burning sensation has to be 48 hours. It has an additional antipruritic
particularly with the 25% lotion. If the skin irritation effect but may cause erythema and conjunctivitis.
is severe, the benzyl benzoate should be washed off. 5. Sulphur: Sulphur can be used as an ointment in a
It may cause irritant dermatitis on the face and scro- concentration between 2% and 10%, and most
tum. The use of analgesia and antihistamines is often commonly, the 6% formulation is used. Sulphur is
advisable before the application. A trial found that highly recommended in that subset of patients who
48% patients treated with topical benzyl benzoate cannot tolerate lindane, permethrin or ivermectin,
were cured as compared with 70% of patients treated though it is substandard to all these agents in efficacy.
with oral ivermectin. The ointment is applied to the entire surface of the
body on two to three consecutive nights. It is cheap further studies need to be performed to prove both
and is a safe choice for the treatment of scabies in the efficacy and safety.
infants, children and pregnant women. Sulphur has
an unpleasant smell and can cause staining of clothes.
In addition, in some cases it may have irritant effects
Drug Resistance Resistance to lindane, permeth-
and variable absorption may result in side effects in rin and crotamiton treatment has been observed.
the kidney. In El Salvador, Peru, Panama, New Zealand, Egypt
6. Monosulfiram: It is used in an emulsion form which and United States, resistance to lindane has been
is applied all over the body after a bath. It is recom- recorded. In vitro evidence of resistance to permeth-
mended that this should be applied once a day on two rin was reported in recurrent crusted scabies. A recent
or three consecutive days. The use of alcohol should study highlighted the in vitro tolerance of Sarcoptes
be strictly avoided during treatment to avoid severe scabiei mites to ivermectin in scabies-endemic com-
reactions. munities. In such circumstances, a cocktail of lindane
7. Malathion: This is an organophosphate insecticide
and benzyl benzoate or permethrin can be used.
which is not currently recommended for the treat-
ment of scabies due to its severe adverse effects.
8. Pimecrolimus: It is a class of immunomodulatory Type-Specific Treatment The basic principles of
drugs and a recent report suggests that it appears to treatment of scabies include the establishment of a
be effective in the treatment of eczema on keratinised diagnosis of scabies and the decision regarding a
skin. A case report highlights that nodular scabies suitable medication. If the treatment is topical, the
treated with topical pimecrolimus showed a marked
whole body should be treated, from the neck to the
improvement after therapy.
9. Ivermectin (systemic): It is used as a treatment of
toes in adults and including the head and face in
choice for a large number of endoparasites (nema- babies. It is also necessary to treat all the direct
todes) and ectoparasites (insects, Sarcoptes scabiei contacts of the case. Follow-up of treated cases
[0.2 mg/kg in a single dose], Pediculus humanus, should be carried out at 1 and 4 weeks after scabi-
Demodex folliculorum and Cheyletiella spp.). Mul- cidal treatment. In addition to scabicidal treatment,
tiple doses are used repeatedly for the treatment of antipruritic agents such as antihistamines may be
Norwegian scabies (200 μg/kg along with kerato- necessary to alleviate itching. Furthermore, suitable
lytics), and in immunocompromised patients. More antibiotics can be used if secondary bacterial infec-
than 98% of the oral dose of ivermectin is excreted tion is present.
in the faeces and it is also metabolised in the liver.
A study conducted on 1153 scabies infested prison- 1. Crusted scabies: Most cases of Norwegian scabies
ers revealed that a single dose of ivermectin cured need to be admitted to the hospital for treatment.
88% of recipients after 4 weeks and showed 95.5% Multiple doses of oral ivermectin may be required in
efficacy after 8 weeks. Some trials highlighted that a addition to topical agents which should be applied all
single dose of 200 μg/kg of oral ivermectin is as effec- over the body. A cure is generally attained after three
tive as traditional topical applications such as benzyl consecutive treatments with topical applications.
benzoate, lindane and permethrin for the treatment However, in some cases, additional treatments such
of ordinary scabies. It is likely a second dose after 1 as keratolytics (5–10% salicylic acid in petrolatum)
week may be required in many patients. The adverse will be required to increase the penetration of scabi-
effects may include anorexia, asthenia, headache, cides. Decayed nails should be trimmed and brushed
arthralgia, myalgias, fever, eosinophilia and macu- with a scabicidal agent. Ten per cent precipitated sul-
lopapular rashes. Due to the limited data on safety, phur in petrolatum is more reliable than permethrin
ivermectin should not be used in children weighing in this setting. Oral ivermectin can be used alone, but
<15kg or during pregnancy or lactation. One study is more effective when used in combination with topi-
suggested a possible neurotoxicity in the elderly. The cal treatment.
resistance of scabies mites to ivermectin has been 2. Scabies in children: A total of 2–10% sulphur in pet-
reported in two cases. rolatum can be used in infants and 5% permethrin
10. Ivermectin (Topical): It has been tested in a few open cream can be used in infants older than 2 months.
label studies; in the most recent one, two applications Crotamiton is also recommended for use in babies
of 1% ivermectin (400 μg/kg per dose) in a solution and toddlers. In infants, the use of ivermectin and lin-
of propylene glycol, spaced 1 week apart, had 100% dane are not advisable. A case report demonstrated
success in treating scabies in adults and children that when oral ivermectin was used in combination
as young as 1 year old with no side effects. Again, with lindane and keratolytics, an 11-year-old girl
with crusted scabies was cured without any side are because of reinfection from untreated con-
effects. A 12.5% benzyl benzoate emulsion can also tacts. It has also been suggested that pruritus can
be used in children. temporarily worsen after treatment secondary to
3. Scabies in pregnant and lactating women: Six per cent the massive death of mites and the release of their
sulphur precipitate/crotamiton are the drugs of choice
toxic products.
in pregnant women and lactating women. Use of iver-
mectin, permethrin (category B) and lindane should
be avoided. SUMMARY OF THERAPY IN SCABIES The
4. Nodular scabies: The use of a scabicide followed by summary of evidence-based treatment is given in
intra-lesional steroids is recommended for the treat- Figure 21.10. Some general treatment tips are given
ment of nodular scabies. Corticosteroids can be rec- in Box 21.1.
ommended if the nodules persist after repeated treat-
ment. A recent report demonstrated that nodular
scabies was cured by topical pimecrolimus.
First line
Second line
Pimecrolimus+ (nodular scabies)
Supportive therapy
• Keratolytics
• Antipruritics
• Antibiotics (infection)
TREATMENT
Topical Therapy Permethrin and malathion are
effective in the treatment of head lice, whereas syn-
ergised pyrethrins are slightly less effective. A recent
Figure 21.12 Secondary infection with crusting on the study found that out of five head lice treatments
scalp with eczematisation on the neck used in vitro against lice that had previous exposure
(plica polonica). to permethrin and pyrethrins, 0.5% malathion was
the most effective pediculicide and ovicide, killing
2. Excoriations, crusts and secondarily impetiginisation all the lice and eggs within 10 minutes. Also effec-
(Figs 21.12 and 21.13): These lesions are seen com- tive was 1% permethrin, which killed all lice in
monly on the neck, forehead, face and ears. In the
about an hour. The ovicidal activity of permethrin
extreme cases, the hair over the entire scalp becomes
a confluent, purulent mass of matted hair, lice, nits,
was 73% in its diluted form and 90% in its non-
crusts and purulent discharge, so-called plica polon- diluted form, demonstrating that permethrin should
ica. This can result in alopecia (Fig. 21.13) be used on dry hair. One per cent lindane was found
to be the slowest-acting pediculicide and the least
effective ovicide.
Systemic Therapy
Ivermectin The drug is pediculicidal, but only
when the lice takes a blood meal. Apart from the
standard dose (Table 21.2) of ivermectin, three
doses of 12 mg given every 7 days, has also been
used to eradicate body lice in the homeless adult
population in France. It is not approved by FDA for
patients with a weight under 15 kg.
A recent study (Chosidow et al., 2010) has
found that for difficult-to-treat cases of infestation
with head-lice infestation, oral ivermectin, given
twice at a 7-day interval, had superior efficacy as
compared with topical 0.5% malathion lotion, a
finding that suggests that it could be an alternative
treatment.
B vitamins in the louse. There are two combinations CONCLUSION The best treatment depends on
proposed for the use of this oral drug. local patterns of resistance. Due to the absence
of these data in India, we rely on western data.
• Combination of 1% permethrin cream and oral TMP
(10 mg/kg/d based on TMP for 10 days in two divided
Resistance can increase if the same formulation
doses) has been used for an extended period of time.
• Combination of 1% lindane shampoo plus oral TMP Resistance has been reported to occur with per-
(8 mg/kg/d based on TMP for 12 days in two divided methrin, synergised pyrethrins and lindane. Most
doses) treatment failures can be attributed to poor tech-
nique, non-compliance or reinfection. As there is
Further studies need to be performed to fully evalu- no product that kills 100% of the eggs; all patients
ate the role of oral TMP as an adjunctive treatment. should be retreated in 1 week’s time to eradicate
Use of louse repellants is another approach to the mature eggs.
minimise infestation. Piperonal is twice as effec- Although the American Academy of Pediat-
tive as DEET (N,N-diethyl-m-toluamide) in a body rics prefers malathion, a European study favours
louse model. Slow-release citronella has some effect the use of oral ivermectin over malathion. In India,
but may cause scalp irritation. in the absence of malathion, ivermectin is a good
The search for newer drugs has focused on option; though it is not FDA approved less than
newer, non-toxic methods of intervention such as 15 kg. Although transmission from fomites has not
5% benzyl alcohol, 4% dimethicone lotion and suf- been proven, it is still recommended to wash, dry
focants. Recently spinosad has been approval for clean, vacuum or isolate (in a sealed plastic bag for
use in patients greater than 4 years of age. 2 weeks) items such as hats, combs, brushes and
linens.
Future Therapies The newer therapies target In Table 21.2, we have excluded pyrethrins as
components of the nit sheath, which is an insolu- they are not available in India. The current recom-
ble polymer that acts as a glue to attach the egg mendations for treatment in order of decreasing
case to the hair shaft. Potential therapeutic agents, efficacy include (i) permethrin 1% cream followed
including proteases, denaturants, β-sheet breaker by (ii) lindane 1%, (iii) pyrethrins with piperonyl
proteins and small protein inhibitors of sheath butoxide and (iv) malathion 0.5%. Dimethicone is
formation. a safer but probably less efficacious options.
line of therapy.
General measures
An evidence-based management of P. capitis is • Laundering (>60°C—10 min)
depicted in Figure 21.14. • Seal mattress for 3 wk
Insecticidal agents
PEDICULOSIS CORPORIS Topical agents
The adult body louse (Pediculosis humanis) lives on • Malathion 0.5%, carbaryl 0.5%, permethrin 5%+
and lay eggs in clothing and not directly on the human Systemic agents
skin. Body lice are most often found in the homeless, • Oral ivermectin+
refugees, beggars and in people staying in generally
unsanitary and/or crowded living conditions.
• Petroleum jelly+
• Mechanical removal+ AETIOLOGY Fleas (dog or cat), mosquitoes,
• Physostigmine 0.25%/1%+ bedbugs, lice, scabies or mites (fowl, grain, grass)
can be implicated in most cases. In India, the most
common cause is mosquito bite. While cimicosis
Second line (bed bugs) is discussed later in the chapter the other
causes are enumerated in Table 21.3.
Hymenoptera • Bees, wasps and ants • Mild: Mild wheal and flare reactions with
variable oedema persisting <24 h
• Systemic reactions: Vomiting, diarrhoea,
generalised oedema, dyspnoea,
hypotension and collapse. Rarely, it can be
life-threatening
• Delayed allergic reactions: They occur within
hours to 2 wk following the sting and
have symptoms similar to those of serum
sickness with urticaria accompanied by
lymphadenopathy and polyarthritis
Diptera (flies) • Botfly (Dermatobia hominis) can cause myiasis • Most commonly there is immediate pruritic
• Simulium or black fly (Onchocercosis) wheals followed by itchy, red papules
• Sand fly carries Leishmaniasis • Myiasis: There is a painful furuncle that
occurs when a fly deposits parasitic larvae on
human skin
• Onchocerciasis: Facial oedema, subcutaneous
nodules and iritis
Siphonaptera (fleas) • Human flea (Pulex irritans) • These bites are typically evident as grouped
• Oriental rat flea (Xenopsylla cheopis) which urticaria papules, some with a central
carries Yersinia pestis (plague) and Rickettsia punctum
typhi (endemic typhus)
Mites • Cheyletiella mites (walking dandruff ) • They cause pruritic dermatitis in humans
who handle pets
• House mouse mite • It can cause an extremely pruritic papular
bites
• Scabies mite (Sarcoptes scabei) • Already discussed
• The red mite (Chigger or Trombiculidae) • Chiggers can transmit scrub typhus
(Rickettsia tsutsugamushi), leaving a black
eschar at the bite site, pneumonitis and
constitutional symptoms
• Demodex folliculorum
Ticks • They are found in trees, grass, bushes or on • Tick bites are painless and are recognised
animals (dogs, cattle). After attaching itself later on when there is itching or when
to the human skin, the female tick feeds, the engorged tick is found. Other features
becomes engorged after 7–14 d, and then that can be seen include urticaria, eschar
drops off formation and granulomatous reaction to
insect bites
• Minor or major constitutional symptoms
can be associated with early stages of
Lyme disease. Multiple symptoms can
accompany both the early-disseminated
disease and late-stage disease, depending
on which system is involved (CNS, cardiac or
musculoskeletal). Very rarely, children can
develop a reversible flaccid paralysis that
starts after the tick has been attached for
several days
MOSQUITO BITES
Allergic reactions to mosquito bites occur due to sen-
sitisation to mosquito salivary proteins. Mosquito
saliva-specific immunoglobulin IgE, IgG antibodies
and T-cell-mediated delayed type hypersensitivity
reaction appear to be involved in the pathogenesis.
Culex quinquefasciatus, Aedes aegypti and Aedes
vexans are the three most important species of mos-
quitoes worldwide.
A recent study found that mosquito bites were
more commonly seen in females and 50% of cases
had a personal history of atopy. The average age of
Figure 21.20 Eczematous reaction which in Indian onset of this reaction was 5.7 years (range 2–58)
skin causes post-inflammatory and the patients were desensitised by an average of
hyperpigmentation. 9.5 years of age.
CLINICAL FEATURES The reaction to mosquito Other uncommon reaction include anaphy-
bites is determined by previous exposure, and the lactic reactions, serum sickness-like illness, bullae,
sequence of events following multiple bites was elu-
cidated by Mellanby (1944, 1946)
• Stage 1 (induction of hypersensitivity): In an individual
not previously exposed, the bites produce no response.
• Stage 2 (delayed skin reactions): With subsequent
bites, a delayed reaction occurs (pruritic wheals) which
develop approximately 24 hours after the bites and
persist for several days.
• Stage 3 (immediate skin reactions and delayed reactions):
After repeated bites for several weeks, the response
changes, with the appearance of an immediate wheal at
the bite site. This resolves after about 12 hours, to be
replaced by the delayed reaction. (papule).
• Stage 4 (immediate reactions): Further exposure provokes
the immediate reaction, but not the delayed response.
• Stage 5 (no reaction): Eventually, tolerance is acquired,
and no reaction occurs.
• Elimination of insects
• Use of repellants (DEET, permethrin)
• Botanicals oils+
Prevention • Fleas (lufenuron, fipronil, Imidacloprid)^
2. In severe anaphylaxis with hypotension and poor parasite in the faeces of the host. On humid soil or
peripheral circulation, epinephrine should be admin- sand, they hatch giving rise to rhabditiform larva
istered intravenously in a dilution of 1:10,000 (1 mg = which form filariform larva which penetrate unpro-
10 mL) in a bolus dose of 0.1 mg until symptoms tected skin. Through the circulatory system, the lar-
improve. An intravenous line should be started. If the
vae lodge in the small intestine. Eggs, as well as the
patient does not respond to initial measures, critical
care referral is essential. These measures include the
larvae, can be transported by flies, increasing their
administration of oxygen, intravenous aminophylline dissemination. The human skin can be penetrated
and inhaled bronchodilators. by mud, dirt or, especially, sand. They are capable
3. Antihistamines should be administered as an adjunct of invading the skin through follicular pores or
to epinephrine because their effect is not immediate. sweat glands where they could remain for a long
4. Steroids have a delayed onset of action and are not time and lead to folliculitis. Usually, they migrate
the first-line drugs for treating a severe systemic reac- through the epidermis at speeds that vary from a
tion. However, unless medically contraindicated, few millimetres to centimetres per day. Rarely, they
they should be used to prevent continued reaction in may also penetrate the dermis.
all but the mildest allergic reactions. The treatment
should begin with 100 mg of hydrocortisone given IV
every 6 hours and the patient should be discharged on CLINICAL FEATURES
a dose of 30 mg of prednisone per day, tapering over 1. Larva migrans caused by Uncinaria: Skin penetration
3–7 days as symptoms dictate. is usually asymptomatic. The infestation presents
5. Immunotherapy with insect venom is effective and with the formation of a pruritic papule associated
should be considered mandatory for patients who with an erythematous track that follows an erratic
have had an immediate systemic reaction to an insect course. This lesion is usually intensely pruritic,
sting. Commercial venoms and fire ant extract can be and it can cause burning or pain (Fig. 21.25). The
used for diagnosis (skin testing) and desensitisation. most commonly involved areas are the soles, hands,
Adults with a previous systemic reaction to a sting gluteus and back.
and a positive venom test will have a similar reaction 2. Larva migrans caused by Gnathostoma (Gnathostomi-
in approximately 50% of instances if stung again. asis): The clinical manifestations vary depending on the
After immunotherapy, a re-sting will elicit a systemic organ involved; the digestive and genitourinary tract,
reaction in less than 5% of patients. kidney, lungs, brain, eyes and ears may be affected.
Skin is the most frequently involved organ and the easi-
est to detect and present in the following forms:
MISCELLANEOUS CONDITIONS
LARVA MIGRANS
(LARVA MIGRANS SYNDROME)
Larva migrans or creeping eruption is an infestation
of the skin by the nematode larvae. These worms
normally parasitise the intestine of other animal
species. The nematode cannot complete its life cycle
in man. As the worm migrates in the epidermis, it
produces a characteristic lesion.
COURSE This is a self-limited disease and humans TREATMENT Emetine and dehydroemetine are
are ‘dead-end’ hosts. Most larvae die and the lesions the drugs of choice. Emetine is given in a dose of
resolve within 4–6 weeks. 1 mg/kg/d for 10 days. Dehydroemetine is given IM
and its dose should not exceed 60 mg/d, because of
MANAGEMENT The best way to prevent cuta- cardiac effects.
neous larva migrans (CLM) is to ban dogs from Metronidazole may be given orally, in a dose
beaches or wear shoes while walking on the beach of 30–40 mg/kg/d, for 21 days. Iodochlorohydroxy-
and to lie on the sand only on tide-washed areas or quinolein 0.25 g can be given 3 times a day for 2–3
on a mattress (a towel does not give enough protec- weeks along with emetine and dehydroemetine.
tion). Symptomatic relief can be provided by topical
application of a corticosteroid preparation under MYIASIS
occlusion.
Myiasis is an infestation of tissues by the larval form
Although the human host is a ‘dead end’ in the
of non-biting dipterous insects (flies). Species of flies
life cycle and this disease is self limiting, spontane-
involved in myiasis include the genera Dermatobia
ous remission takes up to 12 weeks and intervention
(human botfly), Cochliomyia (screw worm), Cordy-
is essential. This includes administration of topical
lobia, Chrysomya, Cuterebra (rodent or rabbit bot-
or oral antihelminthics (albendazole, thiabendazole
fly), Oestrus (sheep botfly), Gasterophilus (horse
and ivermectin). The regimens include:
botfly), Hypoderma (warble fly), Phaenicia (also
• Topical thiabendazole 10–15% cream, applied twice known as Lucilia) (blowfly) and Wohlfahrtia (flesh
to thrice daily, for 5–10 days fly), among others. In Asia, the common causes are
• Oral albendazole in a dose of 400 mg daily for 3–5 days Chrysomya and Wohlfahrtia and in Africa, Cordy-
• A single dose of 12 mg of oral ivermectin lobia and Chrysomya.
MODE OF TRANSMISSION The mode of trans- removal of the human botfly from pregnant women
mission is different for different species. The human involves surgical removal using a cruciform incision.
botfly deposits its eggs on a mosquito or other The three-step process is as follows:
blood-feeding insect, which then transfers them to • Aesthetising the area around the aperture (which
effectively paralyses the larva) with an injection of
the host. Cordylobia species deposit their eggs onto
1% lidocaine.
moist clothing, blankets or sand. The larvae pen- • Covering the breathing hole with a sterile occlu-
etrate the skin after contact with the host. sive ointment (polymyxin B in this case) to suf-
Other organisms deposit their eggs directly on focate the larva.
open wounds or orifices. In some cases, the larvae • Placement of a cruciform incision slightly off centre
move about in the subcutis (migratory myiasis), from the breathing hole to extract the whole larva.
mimicking the pattern of cutaneous larva migrans.
Miscellaneous Agents Camphor (in a concentra-
This is caused by Hypoderma bovis (warble fly),
tion of 1:0 and 1:1) demonstrated a 100% mortal-
whose normal hosts are cattle, or Gasterophilus intes-
ity rate of the Oestrus ovis (sheep nasal botfly) lar-
tinalis (horse botfly), which normally infects horses.
vae. Essential oil of betel in a concentration of 3%
In wound myiasis (Cochliomyia hominivorax—
and 4% was effective in killing 100% of the larvae
New World screw worm), the larvae initially consume
(Chrysomya).
necrotic debris but may proceed to feed on normal
tissue. Furuncular myiasis occurs following the
penetration of normal skin by the larvae. A pruritic BEDBUGS (HEMIPTERA)
papule develops at the site. This slowly enlarges over This small blood-sucking insect was largely eradi-
several weeks into a domed nodule (resembles a cated in developing countries around the 1950s sec-
furuncle). The lesion has a central pore through which ondary to the widespread use of DDT. Within the
the posterior end of the larva protrudes intermittently. past 3 years, 500% increase in the number of cases
The larva can be induced to exit the lesion by covering of bedbug infestations have been reported from the
this exit with pork fat or petrolatum. United States and Europe.
The factors for this increase include, the fre-
TREATMENT quency and ease of international travel, their non-
General Measures To prevent infestation by dependence on the surrounding environment for
Cordylobia spp., people should avoid wearing reproduction, survival time of up to 1 year without
damp clothing or resting in sandy areas and cloth- a blood meal and the ideal environment prevalent
ing can be sun- or heat-dried and/or pressed Insect in urban cities. The sites of transfer include shelters,
repellents can be used to keep mosquitoes carrying hotels and apartment units.
larval eggs away.
Insect: Flattened dorsolaterally, with an ovoid body.
Specific Treatment Most treatment recommenda-
The light to red brown bedbug is wingless, and the adult
tions are based on in vitro experiments or case studies. is typically about 6 mm in length.
1. Furuncular myiasis: The various options include sur-
gical debridement; occlusion/suffocation (i.e. with
petrolatum, liquid paraffin, beeswax, nail polish, LIFE CYCLE/MODE OF INFECTION The life
heavy oils); ethyl chloride sprays; lidocaine injections; cycle has five stages and it completes in about 6–8
cryotherapy; chloroform in vegetable oil or ivermec- weeks. The adult bedbug can typically live for 6–12
tin. Treatment consists of the following measures: months. A female lays 200–500 eggs which remain
• Mechanical removal with a haemostat cemented and hatch within 6–10 days at room tem-
• Compression with a pair of wooden spatula on perature. They are extremely robust creatures and
either side of the nodule so that the larva emerges
remain alive in temperatures as low as 7°C, and as
vertically out of the skin, like a ‘grain of rice’
• Mechanical removal with forceps—in some cases
high as 45°C. At homes, bedbugs hide in the dark
under anaesthesia—after applying a small amount crevices of walls, furniture, picture frames, and peel-
of commercially available mineral turpentine) ing wall-paper, the folds of clothing and linens or in
2. Wound myiasis can be cured by surgical debridement the corners of suitcases. There are two separate species
or surgical removal. An effective treatment for the of bedbug, Cimex adjunctus and Cimex pilosellus.
TREATMENT
Management of Bites Bedbug bites are self-lim-
ited and usually resolve within 1–2 weeks without
treatment. Topical steroids may be used to control
inflammation, and antihistamines may be given to
control pruritus in pronounced cases.
Other Measures
1. The patient should be instructed to launder all bed
linen and vacuum clean the furniture to reduce the
number of bedbugs and their progeny in the home.
2. Prevention of bites and infestations. Covering exposed
parts is the simplest way of preventing the bites. The
following measures should be followed:
• Covering entrances to known refuges of bedbugs
with tape or other tightly woven material effec-
tively hampers bedbug mobility.
• Covering bedposts with petrolatum or inserting
bedposts into jars of paraffin oil may help prevent
Figure 21.26 Although the classic clustering is seen it is bedbugs from gaining access to the bed.
by no way specific of bedbugs and can be • Insecticides like pyrethroid class of insecticides are
seen due to other insect bites also. particularly effective in controlling bedbug infes-
tations. A study from India compared effective-
CLINICAL FEATURES Typically, bedbug bites ness of DEET, DEPA (diethyl phenyl acetamide)
occur at night, and the patient awakes with new and DMP (diethylphthalate) against bedbugs. It
lesions. Bite reactions occur on exposed sites such found DEET to be superior to the rest. Mattresses
as the face, neck, arms and hands, with two to three can be treated with many formulations, but only
lesions in a row (‘breakfast, lunch, dinner’; Fig. 21.26). at seams and buttons.
The typical reaction to the bite of is the development • Vacuuming bedbugs is particularly effective, but it
of an erythematous wheal, followed by a firm, reddish does not usually remove eggs effectively because
they are glued to the substrate.
papule. Occasionally a small central haemorrhagic
punctum may be visualised. In unexposed individu-
als, the bite appears as erythematous, pruritic mac- Resistance Resistance to both deltamethrin and
ules while in sensitised individuals, intensely pruritic L-cyhalothrin, two pyrethroid insecticides, as well
papules, papular urticaria or vesicles/bullae may occur. as chlorfenapyr, has occurred in laboratory popula-
Changes secondary to scratching include exco- tions of bedbugs. Moreover, pyrethroid insecticides
riations, eczematous dermatitis and secondary can cause bedbugs to scatter within a home simply
infections. to avoid treated areas.
ACKNOWLEDGEMENTS
The first three authors have contributed to the section on scabies. The images are of Indian patients.
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