Primary pleomorphic rhabdomyosarcoma of the adrenal gland in an adult: A case report
- Authors:
- Chao‑Jun Wang
- Jun Li
- Jie Qin
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Affiliations: Department of Urology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, P.R. China, Department of Pathology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, P.R. China
- Published online on: November 11, 2013 https://doi.org/10.3892/ol.2013.1674
-
Pages:
137-139
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Abstract
A 61‑year‑old female was referred to The First Affiliated Hospital, College of Medicine, Zhejiang University (Hangzhou, China) due to a right adrenal tumor. A pre‑operative transcutaneous fine‑needle aspiration biopsy and right adrenalectomy were performed, and pathological analysis resulted in the diagnosis of pleomorphic rhabdomyosarcoma (RMS). Primary pleomorphic RMS of the adrenal gland in an adult is a rare condition. To the best of our knowledge, this is the first case of pleomorphic RMS of the adrenal gland in an adult diagnosed by light microscopy and immunohistochemical stains.
View References
1
|
Furlong MA, Mentzel T and Fanburg-Smith
JC: Pleomorphic rhabdomyosarcoma in adults: a clinicopathologic
study of 38 cases with emphasis on morphologic variants and recent
skeletal muscle-specific markers. Mod Pathol. 14:595–603. 2001.
View Article : Google Scholar
|
2
|
Ogilvie CM, Crawford EA, Slotcavage RL, et
al: Treatment of adult rhabdomyosarcoma. Am J Clin Oncol.
33:128–131. 2010.
|
3
|
Stock N, Chibon F, Binh MB, et al:
Adult-type rhabdomyosarcoma: analysis of 57 cases with
clinicopathologic description, identification of 3 morphologic
patterns and prognosis. Am J Surg Pathol. 33:1850–1859. 2009.
View Article : Google Scholar
|
4
|
Sultan I, Qaddoumi I, Yaser S,
Rodriguez-Galindo C and Ferrari A: Comparing adult and pediatric
rhabdomyosarcoma in the surveillance, epidemiology and end results
program, 1973 to 2005: an analysis of 2,600 patients. J Clin Oncol.
27:3391–3397. 2009. View Article : Google Scholar : PubMed/NCBI
|
5
|
Stout AP: Rhabdomyosarcoma of the skeletal
muscles. Ann Surg. 123:447–472. 1946. View Article : Google Scholar
|
6
|
Fletcher CDM, Unni KK and Mertens F:
Pathology and genetics of tumors of soft tissue and bone. Soft
Tissue Tumors. IARC Press; Lyon: pp. 146–153. 2002
|
7
|
Charytonowicz E, Cordon-Cardo C,
Matushansky I and Ziman M: Alveolar rhabdomyosarcoma: is the cell
of origin a mesenchymal stem cell? Cancer Lett. 279:126–136. 2009.
View Article : Google Scholar : PubMed/NCBI
|
8
|
Yi X, Long X, Xiao D, Zai H and Li Y:
Rhabdomyosarcoma in adrenal region of a child with hypertension and
fever: A case report and literature review. J Pediatr Surg.
48:e5–e8. 2013. View Article : Google Scholar : PubMed/NCBI
|
9
|
Katayama A, Otsuka F, Takeda M, et al:
Rhabdomyosarcoma discovered in the adrenal region of an elderly
hypertensive patient. Hypertens Res. 34:784–786. 2011. View Article : Google Scholar : PubMed/NCBI
|