Literature DB >> 15791574

Granular cell tumor of the penis: clinicopathologic evaluation of 9 cases.

William B Laskin1, John F Fetsch, Charles J Davis, Isabell A Sesterhenn.   

Abstract

The occurrence of granular cell tumor (GCT) in penile tissue is very rare, with only 9 examples reported to date in the English-language literature. Herein, we describe the clinicopathologic and immunohistochemical findings in 9 additional cases. The patients ranged in age from 20 to 60 years (mean, 42 years; median, 40 years) at time of diagnosis. All penile tumors were solitary and arose in the dermis of the penile shaft (n=4), prepuce (n=3), and corona (n=2). A patient had a history of multiple cutaneous GCTs. Duration of symptoms before surgery ranged from 5 days to 2 years with the presence of an asymptomatic nodule representing the most common tumor-related complaint (n=8). The lesions ranged in size from 0.6 to 2.5 cm (mean, 1.5 cm; median, 1.5 cm). Microscopically, the tumors were moderate to highly cellular and were composed of oval to polygonal-shaped cells with abundant coarsely granular eosinophilic cytoplasm. Tumor cells grew in infiltrating nests, cords, and trabeculae and showed neural (n=2) and vessel wall (n=1) invasion or formed a relatively well-marginated solid nodule. Bland cytological features with only rare cells showing nucleomegaly (n=7) or spindling (n=3) were exhibited by 8 tumors. A tumor demonstrated diffuse nuclear atypia and was classified as "atypical." Mitotic activity ranged from 0 to 8 mitoses (mean, 1.4 mitoses) per 50 high-powered fields with no atypical division figures identified. All tumors tested showed moderate to strong immunohistochemical expression of S100 protein (n=6) and low-affinity nerve growth factor receptor (n=5), which was useful for detecting small deposits of tumor and helpful in evaluating surgical margins. Focal tumor cell immunoreactivity was observed for calretinin (4/6 cases) and glial fibrillary acidic protein (1/6 cases). All patients underwent simple (local) excision of their tumor. Complete follow-up data (mean, 21 years; interval range, 0.5-28 years) were available for 6 patients. No patient experienced recurrence or metastatic spread of tumor although surgical margins were microscopically involved by tumor in 5 cases. Benign GCT involving superficial soft tissue of the penis can be adequately managed by a simple excision. Patients with microscopically involved surgical margins can be clinically followed without immediate additional surgery.

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Year:  2005        PMID: 15791574     DOI: 10.1016/j.humpath.2004.12.011

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  5 in total

1.  Congenital granular cell epulis presents an immunohistochemical profile that distinguishes it from the granular cell tumor of the adult.

Authors:  Marilena Vered; Alex Dobriyan; Amos Buchner
Journal:  Virchows Arch       Date:  2009-02-11       Impact factor: 4.064

Review 2.  Solitary, multiple, benign, atypical, or malignant: the "Granular Cell Tumor" puzzle.

Authors:  Isidro Machado; Julia Cruz; Javier Lavernia; Antonio Llombart-Bosch
Journal:  Virchows Arch       Date:  2015-12-05       Impact factor: 4.064

3.  Vascular invasion demonstrated by elastic stain-a common phenomenon in benign granular cell tumors.

Authors:  Gábor Cserni; Rita Bori; István Sejben
Journal:  Virchows Arch       Date:  2008-12-10       Impact factor: 4.064

4.  Adjuvant radiation therapy for malignant Abrikossoff's tumor: a case report about a femoral triangle localisation.

Authors:  C Marchand Crety; C Garbar; G Madelis; F Guillemin; P Soibinet Oudot; J C Eymard; S Servagi Vernat
Journal:  Radiat Oncol       Date:  2018-06-20       Impact factor: 3.481

Review 5.  Granular cell tumor of the urethra: a case report and literature review.

Authors:  Chun-Xiao Pu; Liang Gao; Yun-Jin Bai; Ping Han
Journal:  Asian J Androl       Date:  2016 Nov-Dec       Impact factor: 3.285

  5 in total

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