scholarly journals Focal fibrocartilaginous dysplasia (FFCD) in the proximal femur causing coxa vara: A unique case report and review of the literature

2016 ◽  
Vol 15 (3) ◽  
Author(s):  
PH Maré ◽  
DM Thompson
2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
Majid Alsahafi ◽  
Mohammed I. AlJasser ◽  
Sunil Kalia ◽  
H. M. Yang ◽  
Alnoor Ramji

Granuloma annulare (GA) is a benign granulomatous skin disorder of unknown etiology. GA is rarely associated with liver diseases. We report a unique case of chronic hepatitis with liver granulomas in a patient with GA. Despite an extensive workup, no clear etiology for the hepatitis was found. Based on the possible immune pathophysiology of GA and the presence of liver granulomas, the patient was treated with prednisone and azathioprine which resulted in complete normalization of the liver enzymes and concurrent improvement of GA. The association between liver diseases and GA is reviewed.


2014 ◽  
Vol 8 (4) ◽  
pp. 1539-1542 ◽  
Author(s):  
BO SUN ◽  
ZHI HONG ZHANG ◽  
XUAN YING CHEN ◽  
SHAN HU HUANG ◽  
ZHI LI LIU

2016 ◽  
Vol 26 (2) ◽  
pp. 133-136 ◽  
Author(s):  
Doreen Siew Ching Koay ◽  
Wei Qiang Leow ◽  
Thuan Tong Tan ◽  
Gabrielle Slapak

The von Meyenburg complex (VMC) is a rare, congenital malformation of the ductal plate. It is typically asymptomatic and usually discovered incidentally. We report a unique case of recurrent life-threatening hepatobiliary sepsis caused by VMC and a review of the literature. A 62-year-old man presented with recurrent episodes of life-threatening hepatobiliary sepsis. Extensive investigations only showed that he has VMCs without any other source of sepsis or underlying immunodeficiency states. Despite prolonged courses of antibiotics which resolved each episode of sepsis, he suffers repeated recurrences of hepatobiliary sepsis. Liver transplantation is now being considered in view of his refractoriness to medical therapy. As VMC can present with severe hepatobiliary sepsis, it is therefore essential to recognise its presence. This case adds to the literature the atypical but life-threatening clinical presentation of VMC.


Neurosurgery ◽  
1990 ◽  
Vol 27 (6) ◽  
pp. 981-986 ◽  
Author(s):  
Richard B. North ◽  
David H. Kidd ◽  
Henry Wang

Abstract None of the more than 180 cases of anterior sacral meningocele reported in the past 150 years has been bilateral, and only two have been associated with occult intrasacral meningocele. We report a unique case of bilateral anterior sacral cysts, communicating with the subarachnoid space, associated with occult intrasacral meningeal and perineurial (Tarlov's) cysts, in an asymptomatic woman. The pertinent clinical and diagnostic imaging literature is reviewed.


2008 ◽  
Vol 215 (4) ◽  
pp. 307-312 ◽  
Author(s):  
Akira Ando ◽  
Masahito Hatori ◽  
Masami Hosaka ◽  
Yoshihiro Hagiwara ◽  
Atsushi Kita ◽  
...  

2016 ◽  
Vol 9 (1) ◽  
pp. 126-133 ◽  
Author(s):  
Hideo Morioka ◽  
Yasuhiro Kamata ◽  
Kazumasa Nishimoto ◽  
Michiro Susa ◽  
Kazutaka Kikuta ◽  
...  

Fibrous dysplasia (FD) is a monostotic or polyostotic benign bone lesion with spindle-cell proliferation in woven bone and stroma. Rarely, cartilaginous differentiation can be seen in the lesions of FD. FD with massive cartilaginous differentiation is called fibrocartilaginous dysplasia (FCD) and is considered a rare variant of FD. Although pathological findings of FD show irregular immature bone formation without osteoblastic rimming in fibrous tissue, and rarely show very small amounts of cartilage, histological images of FCD are said to show that cartilage with a relatively high cell density is present in the majority and that FD-like findings are seen in parts of it. The most characteristic feature of FCD on images is calcification in the lesions reflecting cartilaginous tissue. On the other hand, typical radiographic findings of FD include shadows with a ground-glass appearance and thinning and bulging of the cortical bone, the observation if calcification is not usual. Therefore, in the diagnosis of FCD, differentiation from multiple enchondromatosis, Ollier disease, chondrosarcoma, and chondrosarcoma secondary to FD is necessary, and it seems important to make a careful diagnosis based not only on the pathological findings but also on imaging and clinical findings. Herein, we report on a case of FD of the proximal femur associated with intralesional extensive cartilaginous differentiation in which a pathological fracture occurred during follow-up, with a review of the literature.


Author(s):  
Ramesh Omranipour ◽  
Athena Farahzadi ◽  
Maryam Hassanesfahani

Most of the bone metastasis origination from Follicular Thyroid Carcinoma (FTC) will present as non-solitary and non-isolated. We present an extremely unique case of an isolated and solitary lesion in an unusual site, scapula, originated from FTC presenting incredibly about ten years after the initial successful treatment.


2002 ◽  
Vol 11 (2) ◽  
pp. 167-171 ◽  
Author(s):  
Mafalda Santos ◽  
Eugénio Valente ◽  
António Almada ◽  
José Neves

2012 ◽  
Vol 6 (6) ◽  
pp. 431 ◽  
Author(s):  
Victor A. McPherson ◽  
Michael Ott ◽  
Edward J. Tweedie ◽  
Jonathan Izawa

The overall 5-year survival of patients with urothelial carcinoma of the bladder (UC) is about 78%; however, there are some rare subtypes. One of these is the lipoid cell subtype, which bears a very poor prognosis. Another rare disease entity with a poor prognosis is metastasis to the lower gastrointestinal tract in the form of secondary linitis plastica of the rectum. We describe an extremely rare and unique case of rectal linitis plastica secondary to the rare lipoid cell variant of UC.


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