Concurrent Eosinophilic Solid and Cystic Renal Cell Carcinoma and Angiomyolipoma With Epithelial Cysts in the Setting of Tuberous Sclerosis Complex: A Rare Synchronous Occurrence of 2 Distinct Entities

2019 ◽  
Vol 27 (7) ◽  
pp. 804-811 ◽  
Author(s):  
Woo Cheal Cho ◽  
Katrina Collins ◽  
Laila Mnayer ◽  
Richard W. Cartun ◽  
Jonathan S. Earle

Eosinophilic solid and cystic renal cell carcinoma (ESCRCC) is a recently described distinct renal neoplasm known to occur almost exclusively in female patients with or without tuberous sclerosis complex (TSC). We report a case of ESCRCC with 2 synchronous angiomyolipomas, including 1 angiomyolipoma with epithelial cysts (AMLEC), a rare cystic variant of AML that typically arises sporadically in the absence of TSC, in a 46-year-old woman with TSC. Besides additional copy number alterations identified in ESCRCC via molecular karyotyping, we also report a unique histologic feature of TSC-associated ESCRCC previously not described in detail, with formation of semicircular multinucleated neoplastic giant cells engulfing an additional intact neoplastic cell, simulating emperipolesis. To the best of our knowledge, this is the first reported case of ESCRCC with concurrent AMLEC in a patient with TSC, confirmed through additional genetic testing showing a germline heterozygous mutation in TSC1. Awareness of ESCRCC helps avoid the pitfall of a diagnosis of unclassified renal cell carcinoma, a typically much more aggressive tumor.

2021 ◽  
pp. 106689692199322
Author(s):  
Seyed Mohammad Mohaghegh Poor ◽  
Shivani Mathur ◽  
Karl Kassier ◽  
Janetta Rossouw ◽  
Robert Wightman ◽  
...  

Two sporadic cases of eosinophilic solid and cystic renal cell carcinoma (ESC RCC), at our institution, are presented in this study to contribute to the growing literature on this novel renal neoplasm. The first patient was a 38-year-old female with two synchronous renal masses measuring 3.5 and 1.9 cm on preoperative imaging. The second patient was a 44-year-old female with an incidental renal mass measuring 4 cm. Both patients underwent uncomplicated radical nephrectomies. The 1.9 cm mass in the first patient was consistent with clear cell RCC. The dominant mass in the first patient and the tumor in the second patient had microscopic and macroscopic findings in keeping with ESC RCC including a tan appearance, abundant eosinophilic cytoplasm, and CK20+ and CK7− staining. Both patients had an uncomplicated course following surgery with no evidence of local recurrence or distant metastatic disease for 1 and 2 years for the first and second patient accordingly. These cases contribute to a growing body of literature regarding ESC RCC including, to our knowledge, the first reported case of synchronous ESC RCC and clear cell RCC. Further research about this novel renal neoplasm is needed.


2018 ◽  
Vol 11 (4) ◽  
pp. 962-970 ◽  
Author(s):  
Jeong Hwan Park ◽  
Cheol Lee ◽  
Mee Soo Chang ◽  
Kwangsoo Kim ◽  
Seongmin Choi ◽  
...  

2010 ◽  
pp. n/a-n/a ◽  
Author(s):  
Joseph G. Pressey ◽  
Jordan M. Wright ◽  
James I. Geller ◽  
David B. Joseph ◽  
Christine S. Pressey ◽  
...  

2020 ◽  
Vol Volume 13 ◽  
pp. 12421-12426
Author(s):  
Yun Wu ◽  
Hongru Li ◽  
Xiaoli Yu ◽  
Ming Lin ◽  
Yusheng Chen

2020 ◽  
Author(s):  
Marjorie Gournay ◽  
Frédéric Dugay ◽  
Marc-Antoine Belaud-Rotureau ◽  
Benoit Peyronnet ◽  
Romain Mathieu ◽  
...  

2015 ◽  
Vol 9 (4) ◽  
pp. 209-211
Author(s):  
Andrew Wood ◽  
Fiona Young ◽  
Marie O'Donnell

Angiomyolipoma with epithelial cysts (AMLEC) is a very uncommon renal tumor. AMLEC has a characteristic histological appearance and immunohistochemical staining pattern, knowledge of which should preclude misdiagnosis by pathologists. We present a rare case of an AMLEC which was suspected to be a cystic renal cell carcinoma radiologically. We describe the characteristic immunological staining pattern and ultrastructural features of this lesion and discuss the potential differential diagnoses.


2014 ◽  
Vol 24 (7) ◽  
pp. 1836-1842 ◽  
Author(s):  
M. E. Tyburczy ◽  
S. Jozwiak ◽  
I. A. Malinowska ◽  
Y. Chekaluk ◽  
T. J. Pugh ◽  
...  

2020 ◽  
pp. 205141582095643
Author(s):  
Helen Cui ◽  
Clare Verrill ◽  
Mark Sullivan

Purpose: The purpose of this article is to present the first reported case of a renal tumour classified as tuberous sclerosis complex-associated renal cell carcinoma in the UK and discuss its clinical implications. Case report: A female, aged 65 years, with tuberous sclerosis complex was found on surveillance imaging to have interval growth of multiple right renal tumours up to 19 mm. Right partial nephrectomy was performed. Histology showed multiple tiny angiomyolipomas and a 20 mm tumour classified as tuberous sclerosis complex-associated renal cell carcinoma. These tumour cells showed abundant clear cytoplasm with a branched elongated arrangement encircled in dense smooth muscle stroma. Literature review: Renal cell carcinoma in patients with tuberous sclerosis complex is rare, occurring in approximately 4% of cases. Tuberous sclerosis complex-associated renal cell carcinoma is a relatively new histological entity, having previously been described as clear cell or chromophobe-like, with only one published case series from the USA. These tumours have three histological entities which are distinct from all other renal cell carcinoma classifications. Based on case series, tuberous sclerosis complex-associated renal cell carcinoma tends to occur more often in females, present at a younger age, have multiple tumours, and tend to show an indolent course, although metastases have been reported. Learning points: Patients with tuberous sclerosis complex can develop renal cell carcinoma, though the risk is thought to be no higher than for sporadic renal cell carcinoma. Given the limited literature, more evidence is required to help predict the future behaviour of these tumours. Level of evidence: 5


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