Sclerosing sertoli cell tumor of the testis

Farhat Abbas; Nida Wahid Bashir; Akbar S. Hussainy

Sclerosing sertoli cell tumor of the testis

Farhat Abbas, Nida Wahid Bashir, Akbar S. Hussainy

Section of Urology, Department of Surgery, Medical College, Pakistan

Research output: Contribution to journal › Article › peer-review

13 Citations (Scopus)

Abstract

Sclerosing Sertoli-cell tumor is a rare, sex-cord-stromal tumor of the testis with distinct clinical and pathological features with only 14 such cases reported in contemporary literature. We report such a tumor in a young diabetic and hypertensive male. Serum beta-HCG, alpha-protein and LDH levels were normal. Pathological examination of right radical orchidectomy specimen was consistent with sclerosing sub-type of Sertoli-cell testicular tumor with no invasion. He remains free of disease recurrence at 6 years following surgery.

Original language	English
Pages (from-to)	437-438
Number of pages	2
Journal	Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
Volume	15
Issue number	7
Publication status	Published - Jul 2005

Keywords

Sertoli-cell
Testis
Tumor

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Cite this

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title = "Sclerosing sertoli cell tumor of the testis",

abstract = "Sclerosing Sertoli-cell tumor is a rare, sex-cord-stromal tumor of the testis with distinct clinical and pathological features with only 14 such cases reported in contemporary literature. We report such a tumor in a young diabetic and hypertensive male. Serum beta-HCG, alpha-protein and LDH levels were normal. Pathological examination of right radical orchidectomy specimen was consistent with sclerosing sub-type of Sertoli-cell testicular tumor with no invasion. He remains free of disease recurrence at 6 years following surgery.",

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T1 - Sclerosing sertoli cell tumor of the testis

AU - Abbas, Farhat

AU - Bashir, Nida Wahid

AU - Hussainy, Akbar S.

PY - 2005/7

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N2 - Sclerosing Sertoli-cell tumor is a rare, sex-cord-stromal tumor of the testis with distinct clinical and pathological features with only 14 such cases reported in contemporary literature. We report such a tumor in a young diabetic and hypertensive male. Serum beta-HCG, alpha-protein and LDH levels were normal. Pathological examination of right radical orchidectomy specimen was consistent with sclerosing sub-type of Sertoli-cell testicular tumor with no invasion. He remains free of disease recurrence at 6 years following surgery.

AB - Sclerosing Sertoli-cell tumor is a rare, sex-cord-stromal tumor of the testis with distinct clinical and pathological features with only 14 such cases reported in contemporary literature. We report such a tumor in a young diabetic and hypertensive male. Serum beta-HCG, alpha-protein and LDH levels were normal. Pathological examination of right radical orchidectomy specimen was consistent with sclerosing sub-type of Sertoli-cell testicular tumor with no invasion. He remains free of disease recurrence at 6 years following surgery.

KW - Sertoli-cell

KW - Testis

KW - Tumor

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M3 - Article

C2 - 16197877

AN - SCOPUS:23644456429

SN - 1022-386X

VL - 15

SP - 437

EP - 438

JO - Journal of the College of Physicians and Surgeons--Pakistan : JCPSP

JF - Journal of the College of Physicians and Surgeons--Pakistan : JCPSP

IS - 7

ER -

Sclerosing sertoli cell tumor of the testis

Abstract

Keywords

UN SDGs

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