Literature DB >> 19415959

Paratesticular paraganglioma: a rare cause of an intrascrotal mass.

Ruta Gupta1, R Spencer Howell, Mahul B Amin.   

Abstract

We describe a case of a paratesticular paraganglioma in a 33-year-old man who presented with a scrotal mass and underwent a right testicular exploration. Metastasis is the only definite criterion for diagnosis of a malignant paraganglioma; however, lymphovascular invasion was noted in this case, which warranted a close clinical surveillance. The patient is currently well with no evidence of disease 18 months after radical orchiectomy. Paratesticular paragangliomas are extremely rare tumors with 6 cases reported in English literature. The histogenesis of these tumors is unknown. Though the histology and immunohistochemistry resemble those of paragangliomas at any other location, these tumors raise a plethora of differential diagnoses especially with the more commonly occurring tumors. Herein the relevant histopathologic differential diagnoses are discussed along with a brief review of literature.

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Year:  2009        PMID: 19415959     DOI: 10.5858/133.5.811

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  3 in total

1.  A rare hereditary and metastatic paraganglioma involved in both spermatic cord and testis.

Authors:  Shuoming Luo; Zhenqi Liu; Zhiguang Zhou
Journal:  Endocrine       Date:  2019-02-23       Impact factor: 3.633

2.  Primary paraganglioma of seminal vesicle.

Authors:  Badr Alharbi; Abdullah Al-Ghamdi
Journal:  Int J Surg Case Rep       Date:  2013-07-26

3.  A 'giant' paraganglioma in the testis.

Authors:  Marinos C Makris; Konstantinos C Koumarelas; Apostolos S Mitrousias; Giannos G Psathas; Athanasios Mantzioros; Stratigoula P Sakellariou; Panagiota Ntailiani; Evripides Yettimis
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2014-10-01
  3 in total

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