scholarly journals A Large Rice Body-Containing Cyst Mimicking Infection following Total Hip Arthroplasty: A Case Report

2017 ◽  
Vol 2017 ◽  
pp. 1-4
Author(s):  
Wael Bayoud ◽  
Maroun Rizkallah ◽  
Samuel Georges ◽  
Tonine Younan ◽  
Gaby Haykal

Introduction. Soft tissue mass following total hip arthroplasty raises several differential diagnoses not limited to infection, hematoma, wear debris, malignancy, and bursitis. Rice body formation in the hip region is an uncommon process denoting a chronic inflammation. We report here the second case of its kind in the medical literature of a wide symptomatic rice-like body cyst complicating a total hip arthroplasty. Case Presentation. This is the case of an 82-year-old white female, presenting with a warm, red, and inflated groin five years after revision of right total hip arthroplasty. Surgical intervention reveals a large well circumscribed cyst containing well-organized rice-like bodies. This eventuality was never reported in differential diagnosis of hip periprosthetic soft tissue masses before. Conclusion. This case report helps widening the array of the differential diagnosis in patients presenting with a slow growing soft tissue mass following total hip arthroplasty, making rice-like bodies cyst a valid one to consider.

2016 ◽  
Vol 44 (5) ◽  
pp. 438-441 ◽  
Author(s):  
Alexander H. Jinnah ◽  
Cynthia L. Emory ◽  
Nicholas H. Mai ◽  
Simon Bergman ◽  
Ziyan T. Salih

2021 ◽  
Vol 41 (1) ◽  
pp. 51-53 ◽  
Author(s):  
Miriam Alonso-Carpio ◽  
Alberto Sánchez-García ◽  
Ana Trapero ◽  
Alejandro Ruíz Valls ◽  
Andrea Vicente Pardo

2021 ◽  
Vol 14 (3) ◽  
pp. e237099
Author(s):  
Daanesh Huned ◽  
Juinn Huar Kam ◽  
Lui Shiong Lee ◽  
Raj Vikesh Tiwari

Synovial sarcomas are most commonly localised in extremities, especially in the lower thigh and knee areas. Comprising less than 1% of all malignancies, retroperitoneal synovial sarcoma is very rare with primary synovial sarcoma of the kidney being even more infrequent and difficult to diagnose. We describe a case report of a renal synovial sarcoma in a young adult who was initially managed as a case of Wunderlich’s syndrome secondary to what was believed to be a ruptured renal angiomyolipoma. After biopsy confirmation, the patient was eventually managed with neo-adjuvant chemotherapy followed by a right radical nephrectomy and right hepatectomy. Despite its rarity, synovial sarcoma should be considered as differential diagnosis of a bleeding retroperitoneal soft tissue mass detected in young adults.


2019 ◽  
Vol 5 (4) ◽  
pp. 471-476 ◽  
Author(s):  
Morad Chughtai ◽  
Linsen T. Samuel ◽  
Alexander J. Acuña ◽  
Atul F. Kamath

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