The Suprapatellar Pouch of the Knee and its Disorders
U.H, Deliwalat, H.R, Jadejat, C. I. Rathod*, N. Loya*
“Assistant Professor, Govt, Medical College and Sir T, Hospital, Bhavnagar.
KEY WORDS : Knoo: Arthroscopy
{uprapatellar pouch:
ABSTRACT
Proper recognition and treatment of pathological conditions of the suprapatellar pouch of the knee
is dependent on the knowledge of normal pouch anatomy and of the various conditions which affect
this area of the knee and contribute to knee pain. This article includes a comprehensive review of
the surgical anatomy of the pouch, current surgical techniques and review of the common conditions
that have a predilection for this often overlooked area of the knee.
INTRODUCTION
The suprapatellar pouch is a large continuation of Given that arthroscopy of the knee is the most
the synovial membrane of the knee joint proximal common procedure in orthopedic surgery, it is
to the trochlea. Its proximal border is positioned essential to be able to identify and address all
approximately 4cm proximal to the superior border _ potential causes of pathology during this procedure
of the patella, lying deep to the quadriceps tendon [18]. One portion of the procedure that has been
ul given very little attention, which may be responsible
for in-complete post-operative pain resolution in
some eases, is pathology of the suprapatellar pouch.
This article provides an anatomic orientation and
systematic approach to the diagnosis and treatment
of suprapatellar pouch pathology.
Within the anatomic boundary of the suprapatellar
pouch congenital, traumatic, inflammatory, and
nooplastic pathology can exist. Congenital anomalies
include partial or complete suprapatellar plica, with
a reported incidence ranging from 9 to 89% [2-5]
However, its role in anterior knee pain is con’ NORMAL ARTHROSCOPIC ANATOMY
troversial [6,7]. Inflammatory pathology of the
suprapatellar pouch includes both systemic and local
conditions such as synovitis, which may be
secondary to rheumatoid arthritis [8,9] or Crohn's
Disease [10], Traumatic suprapatellar pouch pa-
thology can result from pouch rupture [11-18],
previous surgery [14,15], or the presence of loose
bodies [16] within the pouch. These processes have
the potential to cause inflam-mation and subsequent
arthrofibrosis [17]. Neoplasms that exist in the
suprapatellar pouch include pigmented villonodular
sy-novitis and giant coll tumor, hemangiomas,
synovial chondro-matosis, synovial cysts, and most
commonly lipoma arborescens. There has been no
published data on the rate of incidence of traumatic,
‘The entire suprapatellar pouch can be easily
visualized using a standard 30° arthroscope, Proper
examination of the pouch contents requires
identification of the superior pole of the patella, The
quadriceps tendon should be visualized inserting
into the superior pole. The quadriceps tendon ean
then be visualized proximally, running along the roof
of the pouch to a point approximately 4 cm proximal
to the superior pole of the patella. A measuring probe
can be used to con-firm proper pouch length
( Fig. 1). Alternatively, the surgeon can apply
pressure with his finger to the superior pole of the
patella, which can be visualized arthroscopically. An
additional 2-3 fingers (approximately 4 em) can then
be laid down on the skin to ensure that pouch is of
inflammatory, or neoplastic lesions in tho sufficient length. The walls of the pouch should be
suprapatellar pouch, though case reports exist. smooth with normal appearing synovium
Correspondence address : Dr. Ujjval H. Deliwala
Govt Medical College and Sir'T Hospital, Bhavnagar ~ 364002,
an GUJARAT MEDICALFig. I. A. Normal arthroscopie anatomy of the
suprapatellar pouch. The quadriceps tendon can be
visualized running along the roof of the pouch to
point ap-proximately 4 cm proximal to the superior
pole of the patella, Fig. I B.. Classification system
indicating common structures which cause loss of
suprapatellar pouch volume. a) Type III — Complete
suprapatellar plica (pouch compartmentalization) does
not allow fluid exchange between pouch and knee.b)
‘Type II — Incomplete plica, which are smooth, well
organized structures that allow some communication
of synovial fluid between the pouch and joint. C)Type
I — Inflammatory adhesions, which are randomly
oriented, stringy structures, which often minimally
effect pouch volume.
Figure IL. Estimation of knee volume capacity. a)
Insutflation of the knee with 60 em* of saline will slowly
drip out of a standard 18-gauge needle in a kneo with
normal volume capacity. b) Knees with a significant
volume deficit will result in pressurized backflow
after 60 em® insufflation. ¢). Arthroscopic
imagedemonstrates Hypertrophic synovitis in
‘Suprapatellar pouch in PVNS.. d). Histopathologic
Microscopie appearance of PVNS showing hemo-siderin
Jaden multinucleated giant colls that have osteoclastic
features, and macrophages.
Inability to visualize the quadriceps tendon along
the entire roof of the pouch is abnormal ( Fig. 2a).
Pouch lengths significantly less than 4 cm and visible
adhesions are also abnormal.
PATHOLOGY
3.1. Pl
‘Suprapatellar plica, also known as plica synovialis
suprapa-tellaris, are congenital remnants of the
suprapatellar pouch that can range from minimal
to complete plica, with respective results ranging
from free communication to complete isolation, or
compartmentalization, of the suprapatellar pouch
from the knee joint.
Within the first fow weeks of fetal development, the
knee is a tri-compartmental structure composed of
‘medial and lateral tibio-femoral and suprapatellar
compartments, separated by sy-novial infoldings
[19]. Due to intrauterine mechanical forces, these
membranes involute and a single knee cavity is
attained by the 3rd month of fetal life [6], forming
a freely communicating suprapatellar pouch
‘Synovial plicae refer to the mesenchymal remnants
after failure of complete decompartmentalization of
the knee, and can exist as superior, inferior, medial,
or lateral plica with respect to the patella [2,20].
Though there are a number of classification systems
for suprapatellar plica, including the Dandy [4] and
Zidorn [21] systems, most can be classified based
on the classification de-veloped by Deutsch et al. [22]
who differentiate the plica according to 3 different
types. Type A is a complete plica that isolates the
pouch from the knee joint ( Fig. 2a), Type B is a
complete plica except for a central portal, which in
some cases may act as a one way valve [2] (Fig. 2b),
and Type C is an incomplete crescent shaped plica
that is variable in size and confined only to the
superiomedial side 2,4,6,16,22] ( Fig. 2c).
Suprapatellar plica have been shown to exist with
fan in-cidence rate ranging from 9 to 89% [2-5],
however the in-cidence of pathology as a result of
plica is controversial [6,7]. Many believe that the
pathophysiology of suprapatellar plica stems from
an event that leads to inflammation, with resul-tant
alteration of the extensible qualities of the plica
(48)
GUSARAT MEDICAL JOURNAL /PEBRUARY-2010 11.65 to.1[6,23,24]. Thickening, edema, and fibrosis ensue,
which may lead to in-creased force on the articular
surfaces of the patella and medial femoral condyle
and eventual degenerative changes [6,23,24]
Strover et al. [25] arthroscopically demonstrated
the pathome-chanies of the suprapatellar pliea as
impingement of the plica on the medial femoral
condyle and its entrapment between the quadriceps
mechanism and the femoral trochlea, when the knee
is flexed beyond 70°,
It can be argued that alterations in joint volume due
to large suprapatellar plica can cause significant
alterations in fluid distribution and therefore
increased forces on the articular surfaces. Volume
changes may be another etiology of pain due to plica
Regardless of the pathophysiology, suprapatellar
plica can become pathologic and produce symptoms.
3.1.1. Clinical presentation
A patient with suprapatellar plica syndrome may
present with chronic, intermittent, dull pain in the
superior portion of the anterior knee and will
describe it as worse with patello-femoral loading
activities, such as descending stairs [5]. Other
symptoms may include knee or suprapatellar pouch
effusion, a feeling of tightness in the superior knee
that is worse with flexion, or a popping sound and
catching on knee flexion and extension (6)
On physical examination, patients may have
tenderness to palpation over the superior pole of the
patella and suprapatellar pouch. Patients may also
exhibit decreased range of motion of the patella in
the inferior direction. Additionally, suprapatellar
plicae may be palpable as a band of tissue between
the superior pole of the patella and the medial
femoral condyle with flexion and extension of the
knee, and is described as having a distinctly high:
pitched snap with manipulation of the knee [5].
Radiographs, arthrograms, fluoroscopy, C'T, MRI,
and ar-throscopy have all been used as tools for the
diagnosis of suprapatellar plicae [26]. Deutsch et
al, [22] described the lateral view, with the knee in
full extension allowing full distension of the pouch,
as the optimal diagnostic view using double contrast
arthrography for the visualization of suprapatellar
plicae [22]. Alternatively, suprapatellar plica are
best visualized on the sag-ittal view as a band-like,
low-signal intensity structure posterior and superior
to the patella on MRI. Arthroscopy is the gold
standard for diagnosing pathological plicae [26]
3.1.2. Treatment
Once the diagnosis of a suprapatellar plica syndrome
is established via history, physical exam, and
diagnostic techniques, either a non-surgical or
surgical approach can be taken. In patients with
symptomatic plieao, non-surgical approaches have
generally been less effective than surgery. Some
reports indicate no long-term improvement with a
nonoperative approach in those with pathologie
plica (27], though others have reported success with
non-operative measures [24]. Non-operative
measures include a period of non-patello-femoral
loading activities, cryotherapy, ultrasound,
microwave diathermy, patellar bracing, and NSAIDs
[28-30]. Some have also advocated the use of intra
plical ste-roid injections with symptomatic relief in
approximately 3 of 4 patients [31]. Ifnon-operative
measures fail, surgical treatment is indicated [32]
3.1.3. Technique: estimation of joint volume
Normal knee volume is approximately 88 em3 per
our volume Intra-articular injection of 60 em3 of
physiologic saline prior to arthroscopy will allow
estimation of joint fluid capacity. Irrigation will
slowly drip out of a standard 18-gauge needle after
60 cm3 insufflation in a joint with normal capacity
(Pig. 8a), However, knees with significant plica or
arthrofibrosis will result in pres-surized backflow
after 60 em3 insufflation ( Fig. 3b). This phe-
nomenon should alert the surgeon that the joint
capacity is abnormal and identification of pathologie
processes including significant plica is warranted,
3.1.4, Technique: arthroscopic evaluation and
treatment
Suprapatellar plieae can be easily visualized using
a standard 30° arthroscope. The arthroscope is
positioned at the superior pole of the patella and
the quadriceps tendon should then be visualized
proximally. If no quadriceps tendon can be
visualized, a complete suprapatellar plica is likely
present. Alternatively, Strover et al. [25] described
(43)using a lateral suprapatellar portal, at least 1 em
proximal to the superior pole of the patella, with a
70° arthroscope situated proximal to the plica while
looking distally toward the patello-femoral joint.
‘This approach allows visuali- zation of the medial
‘edge of the suprapatellar plica and femoral trochlea
from a proximal perspective. Evaluation of the
dynamic relationship between these structures and
the suprapatellar plieae can then be performed
Ifa plica is identified and considered pathologie, it
should be resected in its entirety. Use caution during
resection to prevent damage to the overlying
quadriceps tendon, which should be visualized
during the entire procedure. Electrothermal cautery
is recommended for resection as strict hemostasis
is imperative, The main complication of plicae
resection is hemarthrosis, which is also postulated
as a causative factor in plicae syndrome [29,33,34],
Generally, surgical outcomes for pliea resection have
been good. Bae et al. [5] reported symptomatic
improvement in 84% of patients with arthroscopic
excision of complete suprapatellar plicae. Harrewyn
et al, hada
arthritic changes and 40% success rate in those with
early arthritis [34,35]
5% sue-cess rate with knees without
3.2, Inflammation and arthrofibrosis
Inflammatory pathology of the suprapatellar pouch
includes both systemic and local inflammatory
[8,9],
[10], and trauma. Traumatic
suprapatellar pouch pathology has been noted to
exist as a result of surgery [14,15], or rupture
(ial.
conditions such as rheu-matoid arthritis
Crohn's Disease
Any inflammation within the knee joint, whether
due to local or systemic processes, may result in
arthrofibrosis. This fibrous tissue can entirely
obliterate the pouch in severe cases [17]. Post
operative arthrofibrosis affecting the suprapatellar
pouch has been demonstrated after total knee
arthroplasty and arthroscopy [14,15,36,37]. The
main clinical symptom is stiffness and re-sultant
limitation of flexion [36,38]. A patellar clunk, similar
in character to that heard from an ACL cyclops
lesion, may also be present with flexion of the knee
if the pouch is significantly fibrosed [38]. Boldt et
al, [39] has encouraged the use of ultrasound as a
method to diagnose arthrofibrosis associated with
total knee arthroplasty, where synovial membrane
thickening greater than 3.0 mm and neo-vascularity
are characteristic and easily identifiable findings.
3.2.1. Treatment
In symptomatic suprapatellar pouch fibrosis, both
nonoperative and surgical therapy may be utilized.
Non‘operative therapy consists of physical therapy
and anti‘inflammatory measures, such as NSAIDs
and steroid injections [40,41].
3.2.2. Technique: arthroscopy
The arthroscopic appearance of arthrofibrotic
adhesions is markedly different than that of plicae.
Scar tissue appears un-organized, and often has a
stringy appearance ( Fig. 2c). Findings may range
from a few wispy adhesions to complete obliteration
of the pouch. Surgical therapy consists of
arthroscopic lysis of the fibrous bands [36], which
should be performed without a tourniquet to assure
complete hemostasis. Slow resection with the use of
electrothermal cautery is recommended. Post-oper
ative mobility of the patella in all planes should be
significantly improved and documented. Post
operative care should include sufficient analgesia
for immediate passive range of motion, cryotherapy
and patellar mobilization. Full weight-bearing
should be delayed for approximately 2 weeks to
minimize post-operative inflammation
3.3. Rupture
‘Though rare, a number of cases of spontaneous and
traumatic suprapatellar pouch rupture have been
reported [11,12]. Cases of pouch rupture secondary
to inflammatory arthritis have also been described
{9,13,42]. Once rupture occurs, the synovial fluid
induces inflammation, which causes muscle necrosis
and gran-ulomata [9]. This is followed by the
formation of a pseudo-capsule, which is composed
of dense fibrous tissue with chronic inflammatory
cells and fibrin deposits
‘The potential for rupture of the suprapatellar pouch
is proportional to the intrabursal pressure if the
pouch is isolated from the knee joint, or the
intracapsular pressure if
communication with the knee joint. Both of which
are affected by synovial fluid volume [11], Other
there is free
0)
SAL /PERRUARY-2010 Wl.65 40.1factors that influence the potential for rupture
include change of the inherent properties of the
synovium, such as in patients with chronic synovitis,
trauma, and rapid change in the position of a knee
with preexisting elevated fluid pressure [11,42]. If
rupture occurs, it will tend to be at the apex of the
suprapatellar pouch, as this has been shown to be
the weakest structural point [43]
3.3.1. Clinical presentation
Patients will present with symptoms that mimic
deep vein thromboses, with pain, warmth, erythema,
and swelling of the affected thigh [42]. This is
similar to pseudothrombophlebitis, a term coined for
the symptoms caused by rupture of a popliteal cyst
into the calf [42]. If suprapatellar rupture is,
suspected, it can be confirmed via ultrasound and
MRI [44,45]
3.3.2, Treatment
A nonoperative approach with the goal of decreasing
intra-bursal pressure is recommended. This can
include synovial fluid aspiration, anti-inflammatory
measures (NSAIDs, intra-articular and systemic
steroid, treatment of the underlying disease), and
rest. Initiation of passive range of motion after a
short period of immobilization may decrease the
occurrence of arthrofibrosis. Though surgery is
rarely necessary, it can be utilized if continued
symptoms and arthrofibrosis exist [48] (see
‘Technique: arthro-scopy in arthrofibrosis section)
3.4, Neoplasm
Lipoma arborescens is the most common tumor of,
the suprapatellar pouch, however, other neoplasms
including pigmented villonodular synovitis (PVNS)
and giant cell tumor, hemangioma, synovial
chondromatosis, and synovial cysts are rarely
encountered.
3.4.1, Lipoma arborescens
Lipoma arborescens is a rare, benign synovial
disorder in middle-aged men that has a predilection
for the suprapatellar pouch of the knee [46-49]. It
is named for its characteristic frond-like, or
arborescent, villous projections of fatty tissue within
a villous synovium ( Fig. 4a). Histologically, villous
pro-liferation as well as hyperplasia of the
subsynovial fat results in complete replacement of
some synovial tissue with fat cells projecting into
the villous extensions [49]
Patients may present with chronic, intermittent
joint effusions, motion restriction, and variable pain
[49]. MRI is the imaging modality of choice, with
pathognomonic findings of frond-like synovial villous
proliferation with the same signal density as fat on
all sequences [50] ( Fig. 4b). Arthroscopic resection,
including synovectomy, is the treatment of choice.
Recurrence has been reported, but full resolution
should be expected with repeat synovectomy [51]
3.4.2. PVNS and giant cell tumor
Pigmented villonodular synovitis (PVNS) is a benign
pro-liferative intra-articular disorder of the
synovium that affects the knee 80% of the time [52].
It is thought to be a reactive lesion, but some have
suggested that it may have a neoplastic etiology [53].
Localized nodular synovitis is also known as a giant
cell tumor, and has been described as being the
tenosynovial counterpart of PVNS, often presenting
as a slowly enlarging painless mass [54,55]. Figue
IL shows Arthroscopic image of Synovial hypertrophy
and The histopathology of PVNS includes synovial
hyperplasia, hypervascularity, the presence of hemo:
siderin laden multinucleated giant cells that have
osteoclastic features, and macrophages [56,57]
‘Though rare, there have been a number of reports
that described isolated PVNS in
compartmentalized suprapatellar pouches [2,58-60]
have
Patients with local PVNS and giant cell tumor in
the suprapatellar pouch may present with indistinct
symptoms that suggest internal derangement
[55,61]. MRI exhibits the characteristic decreased
signal intensity of hemosiderin on both ‘Tl and T2
weighted images [62,63]. Synovectomy is the
treatment of choice, either via arthrotomy or
arthroscopy [64,65]. Some authors advocate
radiotherapy to reduce recurrence [66]
3.4.3. Synovial hemangioma
Synovial hemangioma is a rare, benign vascular
tumor arising from synovium [67], and has a
predilection for the knee [67]. Clinical symptoms
include limitations in range of motion, and
intermittent swelling and pain. MRI exhibits dilated
vas-cular spaces with low velocity blood flow
appearing as intra-articular lobulated masses of
intermediate signal intensity on Tl images, and high
intensity on T2 images [68,69]. An-giography can
G1)be used to confirm the diagnosis as well as treat this
condition via embolotherapy [69]. Surgical resection,
either arthroscopic or open, may be required
depending on the extent of the lesion [67-69].
3.4.4. Synovial chondromatosis
Synovial osteochondromatosis is defined as the
presence of multiple intra-articular osteochondral
bodies that arise as a result of proliferative and
metaplastic changes within the synovium [54]. The
otiology is unknown [70]. Patients ean have joint
pain, swelling, and motion limitations [70,71]. The
presence of mul-tiple, uniform, intra-articular,
osteochondral loose bodies on radiographs is
diagnostic. MRI can be used to evaluate the extent
of the synovium involved [49,72]. Treatment consists
of arthroscopic removal of loose bodies and complete
synovectomy [71,73]
3.4.5, Synovial cysts
Synovial cysts are synovial or fibrous lined cystic
masses that may occur as a result of herniation or
distension of synovial membranes in joints and
bursae [74]. They are often associated with trauma
or chronic inflammatory conditions [74]. Though
often asymptomatic, suprapatellar pouch synovial
eysts can present as cystic or firm masses in the
suprapatellar region [75]. Synovial cysts usually
have normal radiographic findings, but are easily
identified on MRI due to their characteristic
appearance of a well-cireumseribed mass with
homogeneous signal intensity,
which is low on T1 and high on T2-weighted images
[74,76]. Cysts are treated with arthroscopic resection
similar to resection of complete suprapatellar plica
(see Technique! arthroscopic evaluation and
treatment of plica).
CONCLUSION
Identification and treatment of pathological
processes of the suprapatellar pouch is necessary
to improve surgical results in patients with
anterior knee pain. Proper identification of
normal anatomic landmarks such as the superior
pole of the patella and the quadriceps tendon are
the cornerstones to thorough arthroscopic
examination of the pouch.
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REFERENCES:
Gosling JA, H.P., Whitmore I, Willan PLT, Human
anatomy! color atlas and text. 4th ed, Toronto: Mosby:
2002. p. 269.
Pipkin G. Knee injuries: the role of the suprapatellar
plica and euprapatellar bursa in simulating internal
dorangoments. Clin Orthop Relat Res 1971374" 161-76.
Patel D. Arthroscopy of the plicae'synovial folds and
their significance, Am J Sports Med 1978:6(6):217-25,
Dandy DJ. Anatomy of the medial suprapatellar plica
and medial synovial shelf. Arthroscopy 1990:6(2)'79°85
Bae DK, Nam GU, Sun SD, Kim YH. The clinical
significance of the complete type of suprapatellar
membrane. Arthroscopy 1998514(8)'830°5.
Schindler O. Synovial plicae of the knev. Curr Orthop
2004:18(3):210-9.
Dandy DJ. Arthroscopy in the treatment of young
patients with anterior knee pain. Orthop Clin North Am
1986:17(2):221°9.
Coulton BL, Popert AJ. Massive extension of the
suprapatellar pouch into the thigh tissues in rheumatoid
disease. Ann Rheum Dis 1986i45(2): 174°5,
Pastershank SP, Mitchell DM, Knee joint bursal
abnormalities in’ rheumatoid arthritis, J Can Assoc
Radiol 1977:28(0):199-203,
Olszewski MA, Manos RE, Weis PJ, Provencher MT.
Knee pain and swelling due to Crohn disease. A case
report. J Bone Jt Surg 2005:87(8):1844°7,
Duncan AM. Arthrography in rupture of the
suprapatellar bursa with pseudocyst formation. Am J
Roentgenol Radium Ther Nucl Med 19741121 (1):88°98
‘MeCabe JP, Gilmore MF. Spontaneous rupture of the
suprapatellar bursa, J Bone Jt Surg Br 1990:72(6):927,
Nahi AM, Scharf, Kleinhaus U, Besser M, Rosenbaum
‘M. Suprapatellar pouch rupture-a rare complication of
rheumatoid arthritis. Rheumatol Rehabil
1980:19(3):161-2.
Gonzalez A. Fat pad entrapment in suprapatellar pouch
following previous arthroscopic resection of
infrapatellar fat pad and medial plica: a rare
complication. J Musculoskelet Pain 2002;9(4):95°8,
Suzuki M, Kakizaki J, Twukeoka T, Teuneizumi ¥, Miyagi
J, Moriya HT. Acase of spontaneous hemoarthrosis after
1 total knee arthroplasty. Mod Rheumatol Jpn Rheum
Assoc 2006:16(4):248+50,
Pipkin G. Lesions of the suprapatellar plica. J Bone Jt
Surg 19505324,
Lindenfeld TN, Wojtys EM, Husain A. Surgical
treatment of arthrofibrosis of the knee, Instr Course
Leet 2000349:211-21,
Owings MF, Kozak LJ. Ambulatory and inpatient
procedures in the United States, 1996, Vital Health Stat
1998(139):1-119.
Ogata §, Unthoff HK. The development of synovial
plicae in human knee joints: an embryologic study.
Arthroscopy 1990:6(4):315-21
Gray DJ, Gardner B, Prenatal development of the
human knee and superior tibiofibular joints. Am J Anat
1950:86(2):285-87,
52)a1
22
23
28
28
30
a2
36
37
38
39
Zidorn ", Classification of the suprapatellar septum
considering ontoge-netic development. Arthroscopy
199218(4):459-64
Deutsch AL, Reanick D, Dalinka MK, et al. Synovial
plicae of the knee. Radiology 1981;141(8):627-34,
“Amatuzzi MM, Fazzi A, Varella MH. Pathologie synovial
plica of the knee. Results of conservative treatment. Am
J Sports Med 1980;1815):486-3.
‘Tindel NL, Nisonson B. The plica syndrome. Orthop Clin
North Am 1992:28(4):613°8,
Strover AE, Roubolamin E, Guirguis N, Behdad H. An
arthroscopic of demonstrating the
pathomechanies of the suprapatellar plica. Arthroscopy
1991:718):808-10.
Kim SJ, Shin 8J, Koo TY. Arch type pathologic
suprapatellar plica, Arthroscopy 2001:17(5):536°8,
technique
Aprin H, Shapiro J, Gershwind M, Arthrography (plica
A noninvasive method for diagnosis and
prognosis of plica syndrome. Clin Orthop Relat Res
1984(183):90-5,
Dupont JY, Synovial plieae of the knee. Controversies
and review. Clin Sports Med 1997:16(1):87-122.
Ewing JW. Plica: pathologie or not? J Am Acad Orthop
Surg 199851 (2):117-21
Fisher RL, Conservative treatment of patellofemoral
pain. Orthop Clin North Am 1986:17(2):269-72.
Rovere GD, Adair DM, Medial synovial shelf plica
syndrome. Treatment by intraplieal steroid injection.
Am J Sports Med 1985:19(6):282°6.
Adachi N, Ochi M, Uchio Y, Kawasaki K, Yamasaki K.
The complete type of suprapatellar plica in a
professional baseball pitcher: consideration of a cause
of anterior knee pain, Arthroscopy 2004:20(9):987-91
Broom MJ, Fulkerson JB. The plica syndrome: a new
perspective. Orthop Clin North Am 1986'17(2):279-81
Hardaker WT, Whipple TL, Bassett IIT FH. Disgnosis
and treatment of the plica syndrome of the knee. J Bone
St Surg 1980;62(2):221°5,
Harrewyn JM, Aignan M, Renoux M, Delbarre F,
‘Synovial folds of the knee (pica synoviales). Treatment
under arthroscopy, Rev Rhum Mal Osteo-artic
1982:490:3°9
views)
Jerosch J, Aldawoudy AM. Arthroscopic treatment of
patients with modorate arthrofibrosis after total knee
replacement. Knee Surg Sports Traumatol Arthrose
2007:15(1):71-7,
Wang JH, Zhao JZ, He YH. A new treatment stratogy
for severe arthrofibrosis of the knee. A review of twenty
wo cases, J) Bone Jt Surg 2006%88(6):1245-50,
Millett PJ, Wickiewice TL, Warren RF, Motion loss after
ligament injuries to the knee. Part II: prevention and
treatment. Am J Sports Med 2001;29 (6):822°8,
Boldt JG, Munzinger UK, Zanetti M, Hodler J
Arthrofibrosis associated with total knee arthroplasty’
gray-scale and power Doppler sonographic findings. AJR
2004:182(2):337-40.
40
50
54
Arya R, Arthroscopic arthrofibrolysis of the knee-results|
of 28 cases. J Arthrose 2003:19(6)'80,
Ayers D, D.D., Johanson N, Pellegrini V. Instructional
‘course lectures, the American academy of orthopaedic
surgeons-common complications of total knee
arthroplasty. J Bone Je Surg 1997:79:278-411
Schapira D, Balbir-Gurman A, Nachtigal A, Nahir AM.
Suprapatellar pouch rupture in acute gouty arthritis.
Isr Med Assoe J 2001:3(9):700-1
Dixon AS, Grant C. Acute synovial rupture in
rheumatoid arthritis. Clinical and experimental
observations. Lancet 1964:16:742°5,
Lawson TL, Mittler 8. Ultrasonic evaluation of
extremity soft-tissue lesions with arthrographic
correlation. J Can Assoc Radiol 1978:29(1):58-61
Nuss R, Kileoyne R, Geraghty S, Wilkins R, Wiedel J
Maneo-Johnaon M. Magnetic resonance imaging
visualization of hemorrhage into a suprapa'tellar pouch
in a child with hemophilia. Am J Pediatr Hematol Oncol
1994;16(2):183°6.
Hallel 7, Lew S, Bansal M. Villous lipomatous
proliferation of the synovial membrane (lipoma
arborescens). J Bone Jt Surg 1988:70(2):264-70
Martinez D, Millner PA, Coral A, Newman RJ, Hardy
GJ, Butt WP. Case report 745: synovial lipoma
cons. Skolet Radiol 1992:21(6):393°6.
‘Myers BW, Masi AT. Pigmented villonodular synovitis
and tenosynovitis a clinical epidemiologic study of 166
srature roview. Medicine 1980:59(3):228:
arbore
ceases and Li
a8
Narvaex J, Narvaez JA, Ortega R, Juan-Mas A, Roig:
Escofet D. Lipoma arborescens of the knee. Rev Rhum
(Engl ed) 1999:66(6):851°3,
Feller JF, Rishi M, Hughes BC. Lipoma arboreacens of
the knee: MR Coventry MB, Harrison Jr EG, Martin
JF. Benign synovial tumors of the knee: a diagnostic
problem. J Bone Jt Surg 1966:48(7):1350-8,
Goldman AB, DiCarlo EF. Pigmented villonodular
synovitis, Diagnosis and differential diagnosis. Radiol
Clin North Am 1988'26(6):1827-47,
Imhof H, Nobauer-Hubmann IM, Gahleitner A, et a
Pathophysiology and imaging in inflammatory and
Dlastomatous synovial diseases. Skelet Radiol
2o02ss1(6):813-83.
Narvaez JA, Narvaez J, Ortega R, Do Lama B, Roca Y,
Vidal N. Hypointense synovial lesions on T2-weighted
images! differential diagnosis with pathologic
correlation. AJR 2003:181(8):761-9.
Nau, Chiari C, Seitz H, Weixler G, Krenn M, Giant:
cell tumor of the synovial membrane! localized nodular
synovitis in the knee joint. Arthroscopy 2000%16(8): B22
Darling JM, Goldring SR, Harada Y, Handel ML
Glowacki J, Gravallese EM. Multinucleated cells in
pigmented villonodular aynovitis and giant cell tumor
of tendon sheath express features of osteoclasts. Am J
Pathol 1997:150(4):1383-93,
63)56
60
61
62
6a
64
Lin J, Jacobson JA, Jamadar DA, Bllis JH. Pigmented
villonodular synovitis and related lesions’ the spectrum
of imaging findings. AJR 1999:172(1): 191-7,
El-Khoury GY, Corbett AJ, Summers TB, Case report
303. A complete plica synovialis suprapatellaris, with
diffuse pigmented villonodular synovitis limited to an
isolated nan-communicating suprapatellar bursa, Skelet
synovitis of the sequestered suprapatellar bursa. Clin
Orthop Relat Res 1994;306:204-8
Kaulbach C, HM, Bruns J, Schafer HJ. Synovial giant
cell tumor of the suprapatellar bursa. Aktuclle Radiol
1991:102):811-26 xxi,
Bravo SM, Winalski CS, Weissman BN. Pigmented
villonodular synovitis. Radiol Clin North Am
1996:84(2):811-26 xxi.
Bhimani MA, Wenz JF, Frassica FJ, Pigmented
villonodular synovitis: keys to early diagnosis. Clin
Orthop Relat Res 2001;386:197-202,
Durr HR, Stabler A, Maier M, Refior HJ. Pigmented
villonodular synovitis. Review of 20 cases. J Rheumatol
2001:28(7):1620-30,
Hamlin BR, Duffy GP, Trousdale RT, Morrey BF. Total
knoo arthroplasty in patients who have pigmented
Villonodular aynovitia, J Bone Jt Surg 1998:80(1):76-82
Ogilvie-Harris DJ, Weisleder L. Arthroscopic
synovectomy of the knee: is it helpful? Arthroscopy
1995:110):91°6.
O'Sullivan B, Cummings B, Catton C, et al. Outcome
following radiation treatment for high-risk pigmented
villonodular synovitis, International journal of radiation
oncology, biology. physies 1995:32(8)°777-86.
66
67
68
69
0
16
Devaney K, Vinh TD B. Synovial hemangioma
a report of 20 cases with differential diagnostic
considerations. Human Pathol 1998:24(7): 797-45
, Sweet I
Cotten A, Flipo RM, Herbaux B, Gougeon F, Lecomte
Houcke M, Chastanet P. Synovial haemangioma of the
knee! a frequently misdiagnosed lesion. Skelet Radiol
1995:24(4):257-61
Greenspan A, Azouz EM, Matthews II J, Decarie JC.
Synovial hemangioma: imaging features in eight
histologically proven casos, re-view of the literature, and
differential diagnosis, Skelet Radiol 1995:24(8): 589-90,
Milgram JW. Synovial osteochondromatosis! 2
histopathological study of thirty eases. J Bone Jt Surg
1977:59(6):792-80)
Crotty JM, Mona JU
‘osteochondromatosis.
1996:34(2):327-842, xi.
Kramer J, Recht M, Deely DM, et al. MR appearance of
idiopathic synovial osteachondromatosis. J Comput
Assist Tomogr 1993:17(6):772°6.
Roulot E, Le Viet D, Primary synovial
‘osteochondromatosis of the hand and wrist. Report of a
sories of 21 eases and literature review. Rev Rhum (Bngl
ed) 1999166(5):256-66,
Steiner B, Steinbach LS, Schnarkowski P, Tirman PE,
Gonant HK. Ganglia and eysta around joints. Radiol Clin
North Am 1996:34(2):395-426 xi-xii,
‘Lee KR, Tines SC, Yoon JW. CT findings of suprapatellar
synovial cysts. J Comput Assist Tomogr 1984:8(2):
296-8.
Sundaram M, McGuire MH, Fletcher J, Wolverson MK,
Heiberg E, Shields JB. Magnetic resonance imaging of
lesions of synovial origin. Skelet Radiol 1986:15(2)
1106.
Pope Jr TL. Synovial
Radiol Clin North
Am