Adenomatoid Tumor of Epididymis: A Rare Case Report

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dc.contributor.authorKaur, Simrat Jiten_US
dc.contributor.authorRani, Shilpen_US
dc.contributor.authorPrabhjoten_US
dc.contributor.authorKundal, Ramesh Kumaren_US
dc.contributor.authorVikramen_US
dc.date.accessioned2019-12-02T10:30:47Z
dc.date.available2019-12-02T10:30:47Z
dc.date.issued2018-01
dc.description.abstractAdenomatoid tumors are rare benign neoplasms of the paratesticular region, most commonly occurring at the tail of the epididymis. We present a case of adenomatoid tumor in a 65 year old male, known case of prostatic adenocarcinoma, who presented in Urology OPD with painless swelling in testis. Bilateral orchidectomy was done with clinical suspicion of testicular carcinoma. On histopathology, diagnosis of adenomatoid tumor of epididymis was made. Due to its rarity, it is important for the physician and pathologist to be aware of this interesting entity in order to make a correct diagnosis.en_US
dc.identifier.affiliationsJunior Resident, Department of Pathology, Government Medical College, Patialaen_US
dc.identifier.affiliationsProfessor & Head, Department of Pathology, Government Medical College, Patialaen_US
dc.identifier.affiliationsSenior Resident, Department of Pathology, Government Medical College, Patiala.en_US
dc.identifier.citationKaur Simrat Jit, Rani Shilp, Prabhjot, Kundal Ramesh Kumar, Vikram. Adenomatoid Tumor of Epididymis: A Rare Case Report. Annals of International medical and Dental Research. 2018 Jan; 4(1): 6-8en_US
dc.identifier.issn2395-2822
dc.identifier.issn2395-2814
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/187693
dc.languageenen_US
dc.publisherSociety for Health Care & Research Developmenten_US
dc.relation.issuenumber1en_US
dc.relation.volume4en_US
dc.source.urihttps://www.doi.org/10.21276/aimdr.2018.4.1.PT2en_US
dc.subjectAdenomatoid Tumoren_US
dc.subjectEpididymisen_US
dc.subjectParatesticularen_US
dc.titleAdenomatoid Tumor of Epididymis: A Rare Case Reporten_US
dc.typeJournal Articleen_US
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