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SECOND EDITION
Dermatology
Essentials
Jean L. Bolognia MD
Professor of Dermatology
Yale Medical School
New Haven, CT, USA
Julie V. Schaffer MD
Professor of Pediatrics
Hackensack Meridian School of Medicine
Hackensack, NJ, USA
Karynne O. Duncan MD
Private Practice
St Helena, CA, USA
Christine J. Ko MD
Professor of Dermatology and Pathology
Yale Medical School
New Haven, CT, USA
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This book and the individual contributions contained in it are protected under copyright by the Publisher
(other than as may be noted herein).
Notices
Practitioners and researchers must always rely on their own experience and knowledge in evaluating
and using any information, methods, compounds or experiments described herein. Because of rapid
advances in the medical sciences, in particular, independent verification of diagnoses and drug dosages
should be made. To the fullest extent of the law, no responsibility is assumed by Elsevier, authors, editors
or contributors for any injury and/or damage to persons or property as a matter of products liability,
negligence or otherwise, or from any use or operation of any methods, products, instructions, or ideas
contained in the material herein.
ISBN: 978-0-323-62453-4
Printed in Canada
The goal of our Dermatology Essentials handbook is to present the broad spectrum of cutaneous
diseases in a manner that is straightforward and logical while at the same time maintaining
a necessary level of sophistication. The text portion of each section is relatively brief and easy
to review, with schematics and tables providing additional and more detailed information.
Throughout the handbook are algorithms that present a practical approach to evaluation,
differential diagnosis, and treatment of skin disorders. The clinical photographs were chosen
with two key objectives in mind – to provide characteristic examples of specific diseases and
to offer key teaching points. It is our hope that this handbook will improve the dermatologic
care of patients and provide clinicians with greater confidence as they approach patients with
cutaneous diseases.
ix
Acknowledgments
We wish to thank all the dermatologists 33.7C, 33.10, 33.11, 34.2A, 34.11B, 35.4,
whose clinical photographs are used in this e35.13, e35.15, e35.17C, 36.6B, e36.19,
handbook as well as the textbook Dermatol- 37.1A, 38.6, 38.8B, e38.10A, e38.10B,
ogy. In particular we thank Kalman Watsky, 39.3A, 39.7A, 39.8B, e39.14A, 40.1, 41.2A,
MD, whose photographs appear throughout 41.5A, e41.10, 42.5C, 42.7B, 42.8B, 42.10,
the book. The team at Elsevier has provided 43.7A, 43.8A, 43.9B, 43.9D, 43.9E, e43.15,
enormous support, in particular Joanne Scott e43.16A, e43.18A, 44.1A, e44.5B, e44.7C,
and Joanna Souch. Charlotta Kryhl also pro- 45.3B, 46.6A, 46.6B, 46.8C, 46.10C,
vided guidance for the project. 46.10D, e46.22, 47.3B, 47.4B, 47.9, 47.10A,
The following were sourced from the Yale e47.14B, e47.15C, e47.24A, 48.1B, 48.1D,
Dermatology Residents’ Slide Collection 48.9, 48.10, 48.11A, 48.11B, e48.14, 49.4A,
(YDRSC): e50.19, e50.21, 51.2C, 51.2E, 51.3B, 51.3D,
1.3C, 1.3F, 1.4Aiii, 1.5B, 1.6Cii, 1.13A, e51.11A, e51.18A, e51.18B, 52.2B, 52.8C,
2.1B, 2.3, 4.8D, 5.7A, e5.12C, 6.4B, 6.9, 53.2B, 53.15, e53.24, 54.14, 54.15A, 54.15E,
6.12A, 6.15, 6.16, 6.17A, 6.17C, e6.18, 54.15F, 54.15G, 54.16, 54.17, 54.18A, 54.19,
e6.20A, e6.21A, e6.22, e6.24, e6.25A, 54.23A, 54.23B, e54.28, e54.29A, e54.31,
e6.35, 7.2A, 7.2B, 7.3C, 7.3D, 7.6A, 7.8, 55.3B, 55.8B, 55.17B, 56.4A, 56.4D, 56.11C,
7.9A, e7.14, e7.19, e7.20, 8.3B, 8.6, 8.8, 56.11D, 56.11E, 56.11G, 56.11H, 56.11J,
e8.10, 9.5A, 9.5D, 9.5E, 9.5G, 9.6A, 9.6B, 56.11K, e56.17, e56.27, 57.6, e57.15B,
9.6C, 9.7, 9.9A, 9.9B, 9.11A, e9.12, e9.13, e59.22 (inset 2), e59.31A, e59.32, Table
e9.14, e9.17A, e9.17C, e9.18, 10.3A, 10.7, 59.3 (insets), 60.9A, e60.21A, e60.22, 61.5,
10.8A (inset), 10.9A, 12.12B, 12.12E, 12.17, 61.9A, 61.9B, 61.12, 61.17, e61.22B, e61.30,
e12.26, 13.2B, 13.2I, 14.1B, 14.1C, 15.1A, e61.31, e61.37, e61.38, e61.40, e61.42, 62.9,
15.1B, 15.2A, 15.2B, 15.6, 16.1B, 16.1C, 62.10, 62.11B, 62.13, 62.15, 62.16, 62.17A,
16.1E, 16.2A, 16.4, 16.7A, 16.7B, 16.8, 16.9, 62.17B, 62.17C, e62.18, e62.19, 63.5, 63.6,
16.10A, 17.3, 17.7C, 17.8, 17.9B, 17.10A, 64.3D, 64.8A, 64.8C, 64.10, 64.13A, 64.13C,
17.12, 17.13D, e17.18, e17.23A, e17.23B, 64.13D, 64.13E, 64.13F, 64.15F, 64.19A,
e17.24A, e17.26, e17.27B, e17.28A, e17.35, 64.25A, 64.25B, 64.25D, 64.25E, e64.26B,
18.1D, 18.8, 18.9C, 18.11A, 18.12A, 18.18, e64.27, e64.57, 65.7, 65.9A, 65.9B, 65.11A,
19.1C, 19.2B, 19.4A, 19.4B, 19.5B, 19.10A, 65.12, 65.14, 65.17, e65.30B, 67.4A, 67.6A,
19.10B, 19.10D, e19.20, 20.2A, 21.5C, 67.6B, 67.6C, 67.9A, 67.9D, 67.9E, 67.9H,
21.6B, 21.7A, e21.12A, 22.1A, 22.1B, 67.11A, 67.11B, 67.13, 68.7A, 68.7C, 69.2B,
22.1C, 22.1D, 22.7A, 22.7C, 23.6A, 24.2B, 69.4A, 69.4B, 69.4C, 69.4D, 69.5A, 69.5B,
24.5B, 24.10, e24.12, e24.16, e24.22, 25.2A, 69.5C, 69.6A, 69.6B, 69.9, 69.13A, 69.13C,
25.2B, 26.3A, 26.5A, 26.6A, 26.6C, 26.8A, 70.1B, 71.1, 71.2D, 71.11, e71.18A, 72.7,
e26.10A, e26.11, 27.3, 27.4, 28.2A, 28.2B, e72.12, Table 72.1 (inset 1), 73.2C, 73.4C,
28.15, e28.17, e28.18, e28.19A, e28.19B, 73.13, e73.24F, e73.27C, 74.7A, e74.26,
e28.21, e28.24, e28.25, 29.3C, 29.4B, 76.1A, 76.1C, 76.1E, 76.5, 76.8, 76.10,
e29.16, 30.6B, 30.12, e30.14, 31.2B, 31.3A, e76.12, e76.13, 77.2, 77.3A, 77.10, 78.1A,
31.4D, 31.5, 31.11C, 31.11D, e31.15A, 78.1C, 78.1D, 78.1E, 78.2C, 78.2D, 78.3B,
e31.15B, 32.6, 32.7A, 33.3A, 33.3B, 33.3D, 78.4, 78.19, e78.22, e78.23, e78.25, e78.29,
33.3E, 33.3F, 33.3G, 33.4A, 33.5, 33.6, 79.2, 79.4A, 79.4B, 79.5, 80.2A, 80.2B,
x
81.4B, 81.7, e81.14, 82.2C, e82.11, 83.6A, 55.3A, 55.4A, 55.4B, 56.6B, e56.14, 57.12,
e83.14, 84.6B, 85.3, 85.4C, 85.6A, 85.16A, 59.6, 61.10C, 61.10D, 61.13, e61.35, 63.7A,
85.22, 85.26, e85.37B, e85.45, 86.2A, 86.2B, 63.7B, 65.5, 65.11B, 68.6A, 68.6B, 69.8,
86.3A, 86.4A, 86.5E, 86.10, 86.11B, 86.13B, e69.18, e71.19, 73.4B, 73.5B, e73.24C, 78.7A,
86.15A, 87.9, 87.12A, 87.14, 88.3A, 88.3C, 78.7B, e81.13, 95.6, 95.9, 95.10 and 95.20.
88.4, 88.6B, 88.6C, 88.7B, 88.9C, 89.2B, The following were sourced from the USC
Acknowledgments
89.6A, 89.8A, 90.1A, 90.2, 90.6B, 90.12, Dermatology Residents’ Slide Collection
e90.15, 91.2, 91.3, 91.4A, 91.5, 91.6, 91.7A, (USCDRSC):
91.8A, 91.9A, 91.11, 91.13, 91.14, 91.15, 4.6, 36.10, 38.1, 51.7C, 54.13, e55.23B,
e91.18, e91.20B, 92.1, 92.4, 92.6, 92.7, e60.16C, e61.36, 64.16A, 64.16B, 64.18,
92.10B, 93.6E, e93.21A, 94.3, 94.4, e94.17, 64.22A, 64.22B, 64.23, e64.33, e65.29,
95.5, 95.11, 95.12, 95.17A, e95.23, e95.24, 71.2C, e71.18B, 82.2A, 85.28, 91.12, 94.11,
e95.25, 96.5, 96.6, e96.13C, e96.14B, 99.1, and e99.16.
99.3A, e99.14, 100.3B, 100.3C and e100.6. The following were sourced from the
The following were sourced from the NYU SUNY Stony Brook Dermatology Residents’
Dermatology Slide Collection (NYUDSC): Slide Collection (SUNYSBDRSC):
e7.13B, e7.23, e7.26, 8.3A, 8.4, 8.5, e8.14, Figure 54.15C.
9.5C, 9.8B, e9.16, e9.17B, e9.24, 11.2C, 12.18, Chapter 58, Nail Disorders – Nail photos
e14.14, e19.17, 20.3, 23.6B, 23.6C, 24.4, are courtesy of Antonella Tosti, YDRSC, Julie
36.5C, e36.13, e36.15, 40.4A, 46.7B, 53.11C, V. Schaffer, and Jean L. Bolognia.
xi
Dedication
To our families, in particular our husbands – Dennis, Andy, David and Peter – who provided
the indispensable support required to complete this book, from serving as sounding boards
to creating quiet time in busy households.
xii
List of Abbreviations
Ab Antibody Dx Diagnosis
ABI Ankle–brachial index DDx Differential diagnosis
ACE Angiotensin-converting DEET N, N-diethyl-meta-
enzyme toluamide
AI-CTD Autoimmune connective DFA Direct fluorescence antibody
tissue disease DHEAS Dehydroepiandrosterone
ALK Anaplastic lymphoma kinase sulfate
AK Actinic keratosis DIHS Drug-induced hypersensitivity
ANA Antinuclear antibody syndrome (also known as DRESS)
ANCA Antineutrophil cytoplasmic DM Diabetes mellitus
antibody DRESS Drug reaction with
ART Antiretroviral therapy eosinophilia and systemic
symptoms (also known as
BB Broadband
DIHS)
BCC Basal cell carcinoma
DVT Deep vein thrombosis
BID Two times daily
EBV Epstein–Barr virus
BSA Body surface area
ECG Electrocardiogram
BUN Blood urea nitrogen
EEG Electroencephalogram
CBC Complete blood count
EGFR Epidermal growth factor
CDC Centers for Disease Control receptor
and Prevention
ELISA Enzyme-linked
CMV Cytomegalovirus immunosorbent assay
CNS Central nervous system EMG Electromyography
CO Carbon monoxide ESR Erythrocyte sedimentation
COPD Chronic obstructive rate
pulmonary disease FDA US Food and Drug
Cr Creatinine Administration
CRP C-reactive protein G6PD Glucose-6-phosphate
CS Corticosteroids dehydrogenase
xiii
HCTZ Hydrochlorothiazide PET Positron emission tomography
HCV Hepatitis C virus PO Per os (oral administration)
HIV Human immunodeficiency PPD Purified protein derivative
virus PUVA Psoralen plus ultraviolet A
List of Abbreviations
xiv
SECTION 1: The Basics
Fungal
Malignant
Protozoal
Benign
Bacterial
Papulosquamous
and eczematous
dermatosis
Viral Metabolic and toxic
insults/trauma
Infectiou
Urticarias and
erythemas
stic
Infl
amm
s
ator
la
er
y Oth
Neop
Autoimmune
connective Genodermatoses
tissue diseases and developmental
anomalies
Autoimmune
bullous diseases
Dermatologic
disorders
Fig. 1.1 Classification scheme for dermatologic disorders. This scheme is analogous to the
structure of a tree with multiple branch points terminating in leaves.
1
EXAMPLES OF LOCALIZED DISTRIBUTION PATTERNS
Distribution pattern
SECTION 1: The Basics
Generalized/
Localized Solitary
disseminated
Extensor surfaces Flexural areas Major body folds Palms & soles Periorificial
(e.g. elbows (e.g. antecubital, (e.g. inguinal,
& knees) popliteal fossae) axillary)
Palmoplantar
psoriasis
Inverse psoriasis
Acrofacial vitiligo
Atopic dermatitis
Plaque psoriasis
Fig. 1.2 Examples of localized distribution patterns. Additional patterns are outlined in Table 1.1.
Generalized lesions are seen in morbilliform drug eruptions and viral exanthems. Photographs, courtesy,
Peter C. M. van de Kerkhof, MD, Thomas Bieber, MD, and Julie V. Schaffer, MD.
lesion that appears pink in a patient with skin presentations with histopathologic findings
phototype I may appear red-brown to violet in illustrate the concept of clinicopathologic cor-
a patient with skin phototype IV. relation (Figs 1.8–1.15).
• The acuteness versus chronicity of the • In an analogy to dermatopathology,
eruption provides additional information the clinician often looks at the patient at
and with experience can often be determined “medium-power” (i.e. 20×), but it is also
without a history; Table 1.7 outlines major important to analyze the patient at low-power
causes of acute eruptions in otherwise healthy (4×), thus appreciating the overall pattern,
individuals. as well as high-power (100×); the latter is
• Given the relative ease of obtaining skin aided by the use of dermoscopy (Figs 1.16 and
biopsies, clinicopathologic correlation is a 1.17). Additional dermoscopic images are in
keystone of dermatologic diagnosis; however, Chapters 88, 92, and 93.
it is important to choose the ideal lesion • With experience, prompt recognition of
(e.g. in an inflammatory disorder, one that is pertinent positive and negative clinical fea-
fresh but well-developed), as well as the most tures often leads to a narrower differential
appropriate type of biopsy (Fig. 1.6). diagnosis rather rapidly, almost akin to a
• For inflammatory disorders, there is a clas- gestalt. However, when initially learning der-
sification schema in which they are divided matology, it is helpful to separately address
into major histopathologic patterns (Fig. 1.7); each of the key elements (see above).
several side-by-side comparisons of clinical
2
LINEAR CONFIGURATION PATTERNS
Fig. 1.3 Linear configuration patterns. Photographs, courtesy, Kathryn Schwarzenberger, MD, Jean L. Bolognia, MD, Edward Cowen, MD, Whitney High, MD, Joyce Rico, MD, Louis
A. Fragola, Jr., MD, and YDRSC.
3
1
Solar lentigines
Patch • lat, circumscribed, non-palpable
F • V itiligo
• >1 cm in diameter • Melasma
Related by size
• Often hypo- or hyperpigmented • Dermal melanocytosis
• Also other colors (e.g. blue, violet) (Mongolian spot)
• Café-au-lait macule
• Nevus depigmentosus
• Solar purpura
• Port-wine stain (early)
Vitiligo
Related by size
• Need to distinguish from vesicle (angiofibroma)
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or pustule
Seborrheic keratosis
• W
hen viewed in profile, it may be • S ebaceous hyperplasia
flat-topped, dome-shaped, filiform, • Small vessel vasculitis
pedunculated, smooth, verrucous,
or umbilicated (see Fig. 1.4)
Cherry angioma
Related by size
by a confluence of papules
Dermal
• Granuloma annulare
• Sarcoidosis
• Hypertrophic scar, keloid
• Morphea
Both epidermal and dermal
• Discoid lesions of lupus
erythematosus
Sarcoidosis
Sarcoidosis
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Table 1.2 Primary lesions – morphological terms. Continued
5
1
Related by size
Herpes simplex
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Bulla • E levated, circumscribed • F riction blister
• >1 cm in diameter • Thermal burn (second-
• Fluid-containing, usually clear or degree)
serous but may be hemorrhagic • Bullous pemphigoid
• May become an erosion or • Linear IgA bullous
ulceration dermatosis
• Bullous fixed drug
eruption
Related by size
• Coma bullae
Bullous fixed drug eruption • Edema bullae
Wheal • T
ransient elevation of the skin due • U rticaria
to dermal edema • Urticaria multiforme
Table 1.2 Continued Primary lesions – morphological terms. Photographs, courtesy, Jean L. Bolognia, MD, Lorenzo Cerroni, MD, Edward Cowen, MD, Louis A.
Fragola, Jr., MD, Whitney High, MD, Joyce Rico, MD, and Kalman Watsky, MD.
7
1
Fig. 1.4 Descriptive terms for topography. Photographs, courtesy, Jennifer Choi, MD, Hideko Kamino, MD,
Reinhard Kirnbauer, MD, Petra Lenz, MD, Frank Samarin, MD, Julie V. Schaffer, MD, Judit Stenn, MD, and YDRSC.
Fig. 1.5 Major types of cutaneous atrophy. Photographs, courtesy, Susan M. Cooper, MD, Fenella
Wojnarowska, MD, Jean L. Bolognia, MD, and YDRSC.
8
SECONDARY FEATURES – MORPHOLOGICAL TERMS
Feature Description Disorders
Crust • D ried serum (serous), blood • E czema/dermatitis (multiple types)
(hemorrhagic), or pus on the • Impetigo
surface • Later phase of herpes simplex, varicella or
• May include bacteria (usually zoster
Staphylococcus) • Erythema multiforme
Secondarily infected
hand dermatitis
Scale • H yperkeratosis • soriasis (micaceous [silvery] scale)
P
• Accumulation of stratum corneum • Tinea (leading scale)
due to increased proliferation and/ • Erythema annulare centrifugum (trailing scale)
or delayed desquamation • Actinic keratoses (gritty)
• Represents a primary rather than a • Pityriasis rosea (peripheral collarette and/or
secondary feature in ichthyoses central scale)
• Seborrheic (greasy)
Psoriasis • Tinea versicolor (powdery [furfuraceous])
• Lamellar ichthyosis (plate-like)
Fissure • L inear cleft in skin • ngular cheilitis
A
• Often painful • Hand dermatitis
• Results from marked drying, skin • Sebopsoriasis (intergluteal fold)
thickening, and loss of elasticity • Irritant cheilitis
Hand dermatitis
Excoriation • E xogenous injury to all or part of • A secondary feature of pruritic conditions,
the epidermis (epithelium) including arthropod bites and atopic
• Usually due to scratching dermatitis
• Neurotic excoriations
• Acne excoriée
Neurotic excoriations
Table 1.3 Secondary features – morphological terms. Continued
9
1
Pemphigus foliaceus
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Ulceration • A deeper defect (compared to an • enous (stasis) ulcer
V
erosion), with loss of at least the entire • Neuropathic ulcer
epidermis plus superficial dermis • Arterial ulcer
• May have loss of the entire dermis • Decubitus ulcer
or even subcutis
• Aphthous ulcer
• Size, shape, and depth of the ulcer
• Ecthyma gangrenosum
should be noted in addition to
characteristics of the border, base, • Ecthyma
and surrounding skin • Pyoderma gangrenosum
Acne scarring
Table 1.3 Continued Secondary features – morphological terms. Photographs, courtesy, Louis A. Fragola, Jr., MD, Jeffrey C. Callen, MD, Julie V. Schaffer, MD, and
Whitney High, MD.
11
1
• Melasma
• Vitiligo
• P etechiae
• Dermal
melanocytosis
Epidermal Dermal
Table 1.4 Use of palpation in analyzing cutaneous lesions. Courtesy, Whitney High, MD.
12
1
DIFFERENT CUTANEOUS BIOPSY TECHNIQUES
B
Saucerization Compound
melanocytic nevus
D
Incisional Pancreatic panniculitis
Fig. 1.6 Different cutaneous biopsy techniques. See next page for figure legend.
13
Fig. 1.6 Different cutaneous biopsy techniques. A Superficial shave biopsy can be performed to
remove the elevated portion of an intradermal nevus or to distinguish a solar lentigo (pictured here) from
lentigo maligna. B Deep shave biopsy (saucerization); performed to remove a compound melanocytic
nevus or atypical melanocytic nevus. C Punch biopsy; performed to examine the dermis (as well as the
epidermis) and the preferred technique for diagnosing cutaneous small vessel vasculitis. D Incisional
biopsy; recommended for determining the specific type of panniculitis. Courtesy, Suzanne Olbricht, MD,
Raymond Barnhill, MD, Kenneth Greer, MD, Frank Samarin, MD, and YDRSC.
SECTION 1: The Basics
$ % &
Perivascular dermatitis Vacuolar/interface dermatitis Spongiotic dermatitis
Superficial Superficial
and deep
' ( )
* + ,
Small vessel vasculitis Nodular and diffuse dermatitis Folliculitis
- . /
Fibrosing dermatitis Lobular panniculitis Septal panniculitis
A B
Fig. 1.10 Psoriasiform pattern. A Psoriasis vulgaris – pink plaques with silvery scale on the
shin; this clinical description utilizes the key elements of color, primary lesion, secondary changes,
and distribution pattern (extensor surfaces) in order to arrive at the diagnosis. B Regular epidermal
hyperplasia and elongated dermal papillae with thin suprapapillary plates and confluent parakeratosis.
The parakeratosis represents the histopathologic correlate of the visible scale. A, Courtesy, Julie V.
Schaffer, MD; B, Courtesy, Lorenzo Cerroni, MD.
A B
A B
16
1
A B
Fig. 1.15 Septal panniculitis. A Multiple red-brown nodules of erythema nodosum on the shins,
admixed with healing bruise-like areas. B Predominantly septal granulomatous infiltrate with formation
of characteristic Miescher’s granulomas. A, Courtesy, Kenneth Greer, MD; B, Courtesy, Christine Ko, MD.
17
ACUTE CUTANEOUS ERUPTIONS IN OTHERWISE HEALTHY INDIVIDUALS
Disorder Characteristic findings
Urticaria • P athogenesis involves degranulation of mast cells with release of
(see Ch. 14) histamine
• Primary lesion: edematous wheal with erythematous flare
SECTION 1: The Basics
• Widespread distribution
• Very pruritic*
• Individual lesions are transient (<24 hours in duration)
• May become chronic (>6 weeks)
Acute allergic • Immune-mediated and requires prior sensitization
contact • Primary lesion: dermatitis, with vesicles, bullae, and weeping when
dermatitis severe
(see Ch. 12) • Primarily in sites of exposure; occasionally more widespread due to
autosensitization
• Pruritus, often marked
• Spontaneously resolves over 2–3 weeks if no further exposure to
allergen (e.g. poison ivy, nickel)
Acute irritant • irect toxic effect
D
contact • Primary lesion: ranges from erythema to bullae (e.g. chemical burn)
dermatitis • At sites of exposure
(see Ch. 12)
• Burning sensation
• Spontaneously resolves over 2–3 weeks if no further exposure to
irritant (e.g. strong acid, strong alkali)
Exanthematous • Immune-mediated and requires prior sensitization
(morbilliform) • Pink to red-brown, blanching macules and papules; may become
drug eruptions purpuric on distal lower extremities
(see Ch. 17) • Widespread distribution
• May be pruritic
• Spontaneously resolves over 7–10 days if no further exposure to
inciting drug
Pityriasis rosea • M ay follow a viral illness
(see Ch. 7) • Primary lesion: oval-shaped, pink to salmon-colored papule or
plaque with fine white scale centrally and peripheral collarette;
occasionally vesicular
• Initial lesion is often largest (herald patch)
• Favors trunk and proximal extremities; may have inverse pattern
(axillae and groin); long axis of lesions parallel to skin cleavage lines
(see Fig. 7.7)
• Spontaneously resolves over 6–10 weeks; exclude secondary
syphilis
Viral exanthems • D ue to a broad range of viruses, including rubeola, rubella,
(see Ch. 68) enteroviruses, parvovirus, adenovirus (see Fig. 68.1)
• Often associated with fever, malaise, arthralgias, myalgias, nausea,
upper respiratory symptoms
• Primary lesions vary from blanching pink macules and papules to
vesicles or petechiae
• Distribution varies from acral to widespread; may have an enanthem
• Spontaneously resolves over 3–10 days
*May have burning rather than pruritus with urticarial vasculitis, and individual lesions of urticarial vasculitis
can last longer than 24 hours.
Table 1.7 Acute cutaneous eruptions in otherwise healthy individuals.
18
1
D
Fig. 1.16 Use of dermoscopy to aid in the diagnosis of four common pigmented
(non-melanocytic) cutaneous lesions. A Pigmented basal cell carcinoma with leaf-like areas
(islands of blue-gray color) at the periphery and a small erosion of reddish color at the left side
of the lesion. B Seborrheic keratosis with typical milia-like cysts (white shining globules) and
comedo-like openings (black targetoid globules). C Angiokeratoma with red-black lacunas
clearly visible as well-demarcated roundish structures. D A dermatofibroma with characteristic
central white patch and peripheral delicate pseudo-network. Dermoscopic features of
melanocytic nevi and melanoma are reviewed in Chapters 92 and 93. Courtesy, Giuseppe
Argenziano, MD, and Iris Zalaudek, MD.
A
Fig. 1.17 Use of dermoscopy to aid in the diagnosis of inflammatory disorders. A By
dermoscopy, classic psoriasis plaques exhibit regular dotted vessels. Continued 19
SECTION 1: The Basics
Fig. 1.17 Continued B The dermoscopic pattern of lichen planus is definitely different from the
previous one. Here, dotted vessels are seen at the border of typical whitish lines and clods, which
closely resemble the Wickham striae found in lichen planus of the oral mucosa. Courtesy, Giuseppe
Argenziano, MD, and Iris Zalaudek, MD.
20
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Lawn Benches Made from Old Bedsteads
All traces of the old cork on the joint can be removed with
sandpaper, leaving it as shown at the left. The cork comes in strips
of about the proper thickness, and wide and long enough to allow for
trimming. The ends of the strip should be beveled to make a ¹⁄₄-in.
lap joint.
A small quantity of the cement is heated over the lamp and six
drops poured on the joint; then with the end of the file, which should
be heated also, it is spread to give an even, thin coating. The
beveled ends of the strip are similarly treated. By working quickly
and carefully, the coating on the joint and strip are brought to a
plastic state by holding in the flame, and the strip is quickly laid in
place. Before the cement has time to harden, press the cork in,
forming a neat joint. Bind a rag around the cork, leaving it until the
cement is thoroughly set.
The corked joint will be too large to go into the joining section of
the instrument. File and sandpaper it to a twisting fit. Though the
cork should be truly cylindrical, it may be tapered a trifle smaller at
the forward end. A coating of tallow applied to the joint will make it
easy-fitting, but air-tight and moisture-proof.
The pads are disks of felt incased in thin sheepskin. After long
usage, they become too hard to make an air-tight fit. Repadding
should, therefore, be anticipated. Shellac will give good results in
putting on pads. It is heated until liquid and poured into the key
recess. The new pad is pressed into the liquid shellac, care being
taken to have it well centered. For different keys, it will be necessary
to use varying quantities of shellac to make the pad sit higher or
lower, as required.—Donald A. Hampson, Middletown, N. Y.
Anyone with a power boat can construct a blower for the whistle
very cheaply. The whistle is attached to a suitable length of pipe,
threaded on each end. The blower is made of two white-pine boards,
1 in. thick, cut as shown at A; a thin piece of leather is cut like the
pattern B, to form the bellows part, and after it is shaped, the edges
of the boards are glued and the leather placed in position, where it is
fastened with tacks driven in about 1 in. apart. The bellows are
fastened to the under side of a seat with screws, and a tension
spring is attached to the bottom of the bellows and the floor of the
boat. A cord is fastened to the lower board of the bellows and run up
through to the cabin roof over suitable pulleys to a handle within
convenient reach of the operator.—Contributed by John I. Somers,
Pleasantville, N. J.
Filling In Broken Places on Enamel
Ordinary putty will not do to fill in cracks or broken spots on an
enameled surface, such as a clockface. Fine sealing wax is much
better, as it hardens at once, takes color without absorbing the oil,
and does not shrink like putty. Use a wax of the proper color to
match the surface as closely as possible. Fit it in and smooth with a
warm, flexible piece of metal, such as a palette knife. Give it one or
two coats of thin color to exactly match the other surface, and
varnish. If the article has not a high polish, the gloss of the varnish
can be cut a little with pumice stone.
A Twisting Thriller Merry-Go-Round
By R. E. EDWARDS
“Stepdime!”
right up; three twisting thrillers for a penny—a tenth of a
was the familiar invitation which attracted customers to
the delights of a homemade merry-go-round of novel design. The
patrons were not disappointed, but came back for more. The power
for the whirling thriller is produced by the heavy, twisted rope,
suspended from the limb of a tree, or other suitable support. The
rope is cranked up by means of the notched disk A, grasped at the
handle B, the car being lifted off. The thriller is stopped when the
brakeplate I rests on the weighted box L.
The Supporting Ropes are Wound Up at the Disk A, the Car is Hooked into
Place, and the Passengers Take Their Seats for a Thrilling Ride, Until the
Brakeplate I Rests on the Box
Manila rope, ³⁄₄ in. or more in diameter, is used for the support,
and is rigged with a spreader, about 2 ft. long, at the top, as shown.
The disk is built up of wood, as detailed, and notches, C, provided
for the ropes. The rope is wound up and the car is suspended from it
by the hook, which should be strong, and deep enough so that it
cannot slip out, as indicated at H.
The car is made of a section of 2 by 4-in stuff, D, 10 ft. long, to
which braces, E, of 1 by 4-in. stuff are fastened with nails or screws.
The upper ends of the pieces E are blocked up with the centerpiece
F, nailed securely, and the wire link G is fastened through the joint.
The seats J are suspended at the ends of the 2 by 4-in. bar, with
their inner ends lower, as shown, to give a better seating when the
thriller is in action. The seats are supported by rope or strap-iron
brackets, K, set 15 in. apart. The box should be high enough so that
the seats do not strike the ground.