Testicular tumors with peutz‐jeghers syndrome

Darrell M. Wilson; William C. Pitts; Raymond L. Hintz; Ron G. Rosenfeld

doi:10.1002/1097-0142(19860601)57:11<2238::AID-CNCR2820571128>3.0.CO;2-C

Testicular tumors with peutz‐jeghers syndrome

Darrell M. Wilson, William C. Pitts, Raymond L. Hintz, Ron G. Rosenfeld

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

123 Scopus citations

Abstract

The case of a 6‐year‐old boy with Peutz‐Jeghers syndrome (PJS), gynecomastia, and multifocal and bilateral testicular tumors is described. Females with PJS are known to be at increased risk for developing gonadal tumors. This case and other reports from the literature suggest that males, as well as females, with PJS are at risk for developing gonadal tumors.

Original language	English (US)
Pages (from-to)	2238-2240
Number of pages	3
Journal	Cancer
Volume	57
Issue number	11
DOIs	https://doi.org/10.1002/1097-0142(19860601)57:11<2238::AID-CNCR2820571128>3.0.CO;2-C
State	Published - Jun 1 1986
Externally published	Yes

ASJC Scopus subject areas

Oncology
Cancer Research

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10.1002/1097-0142(19860601)57:11<2238::AID-CNCR2820571128>3.0.CO;2-C

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AU - Wilson, Darrell M.

AU - Pitts, William C.

AU - Hintz, Raymond L.

AU - Rosenfeld, Ron G.

PY - 1986/6/1

Y1 - 1986/6/1

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AB - The case of a 6‐year‐old boy with Peutz‐Jeghers syndrome (PJS), gynecomastia, and multifocal and bilateral testicular tumors is described. Females with PJS are known to be at increased risk for developing gonadal tumors. This case and other reports from the literature suggest that males, as well as females, with PJS are at risk for developing gonadal tumors.

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Testicular tumors with peutz‐jeghers syndrome

Abstract

ASJC Scopus subject areas

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