scholarly journals Exercise-induced ruptured renal tumour in a young patient with hereditary leiomyomata-associated renal cell carcinoma (HLRCC): a case report

2021 ◽  
Vol 27 (1) ◽  
Author(s):  
Mohamad Fairuz Mohamad Sharin ◽  
Mugialan Pushpanathan ◽  
Arvind Vashdev Jagwani ◽  
Khairul Asri Mohd Ghani ◽  
Saiful Azli Mohd Zainuddin ◽  
...  

Abstract Background Hereditary leiomyomatosis-associated renal cell carcinoma (HLRCC) is rare with only 300 families reported to date worldwide. Despite highlighting renal malignancy, it is infamous for its cutaneous and leiomyomatosis component as the more common cause of presentation. This report is to highlight the rare presentation of HLRCC which occurs in a teenager which is unfortunately complicated with exercise-induced renal tumour rupture. Case presentation A 22-year-old gentleman presented with severe right lower abdominal pain for 4 days, associated with fever and nausea following a session of strenuous exercise. He has first-degree relatives and second-degree relatives from his maternal side who were genetically tested positive for HLRCC. Clinical examination revealed a tender right lumbar and right iliac fossa region. A computed tomography of the kidneys demonstrated a ruptured right renal tumour with a large right renal subcapsular and contained right retroperitoneal hematoma. An emergency right radical nephrectomy was performed, and he recovered well. The histopathological examination was consistent with HLRCC associated ruptured right renal cell carcinoma. Conclusion Identification of this underreported familial malignancy is paramount as the onset of neoplasia occurs much earlier in life. This necessitates screening of family members at a younger age, and the management is followed by life-long surveillance.

2016 ◽  
Vol 33 (2) ◽  
pp. 68-73
Author(s):  
Pedro Miguel Baltazar ◽  
Ana Meirinha ◽  
Raquel João ◽  
João Magalhães Pina ◽  
Hugo Pinheiro ◽  
...  

2015 ◽  
Vol 9 (9-10) ◽  
pp. 654 ◽  
Author(s):  
Aanchal Kakkar ◽  
Mehar C. Sharma ◽  
Manpreet Uppal ◽  
Sunil Chumber

Cystic neoplasms of the kidney are rare, and present a unique diagnostic challenge. We report the case of an elderly male who presented with a large cystic neoplasm, which was a diagnostic dilemma clinically and radiologically. Histopathological examination showed a tumour composed of variably sized tubules lined by atypical cells having large round nuclei with prominent nucleoli. Hobnailing was seen at places. Tumour cells were immunopositive for pancytokeratin, vimentin, CD10, CK19 and AMACR, confirming a diagnosis of tubulocystic renal cell carcinoma (TC-RCC).


2014 ◽  
Vol 21 (3) ◽  
pp. 521 ◽  
Author(s):  
R.M. Kumar ◽  
T. Aziz ◽  
H. Jamshaid ◽  
J. Gill ◽  
A. Kapoor

2014 ◽  
Vol 8 (7-8) ◽  
pp. 536 ◽  
Author(s):  
Zhang Zhiqiang ◽  
Min Jie ◽  
Yu Dexin ◽  
Shi Haoqiang ◽  
Xie Dongdong

The simultaneous occurrence of different histological types of adjacent neoplasms in the same organ is called a collision tumour, and rarely occurs in the kidney. A 63-year-old female presented to the urology department with a 1-month history of a painless hematuria. The computed tomography scans of the abdomen revealed 2 heterogeneous incidental right renal masses. The patient underwent radical nephrectomy including lymphadenectomy without adjuvant therapy. Histopathological examination showed a type 2 renal collision tumour of the papillary renal cell carcinoma with eosinophilic cytoplasm and pseudo stratified nuclei on papillary cores, and chromophobe renal cell carcinoma characterized by large polygonal cells with transparent reticulated cytoplasm and prominent cell membranes, which exhibited sarcomatoid transformation in the local area. Routine follow-up demonstrated no localor distant metastasis signs of recurrence at 20 months.


2018 ◽  
Vol 9 (3) ◽  
pp. 183-185
Author(s):  
Shilpi Shah ◽  
Poornima Vinod ◽  
Mohamed Khayata ◽  
Jason L. Lane ◽  
Vinayak Hegde ◽  
...  

2012 ◽  
Vol 05 (04) ◽  
Author(s):  
Amit Attam ◽  
Arun Kerketta ◽  
Sameer Trivedi ◽  
Udai Shankar Dwivedi

2008 ◽  
Vol 12 (3) ◽  
pp. 99-101 ◽  
Author(s):  
Ho-Yin Ngai ◽  
Lap-Yin Ho ◽  
Tung-Fei Chan ◽  
Hing-Shing So ◽  
Venu Velayudhan ◽  
...  

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