[Foamy carcinoma of the prostate].

Abstract:

OBJECTIVES:We report the first case of prostatic foamy gland carcinoma in the Spanish literature. METHODS:Case of a 69-year-old male who consulted for PSA elevation up to 101 ng/ml. Transrectal ultrasound showed a heterogeneous gland with a hipoechogenic area in the right lobe and possible capsular disruption. Six ultrasound guided needle biopsies were performed. The samples from the right lobe were reported as Gleason 6 foamy cell prostatic adenocarcinoma. RESULTS:Prostatic foamy cell carcinoma is a rare tumor, and so are its bibliographic references. Its cells lack of prominent nucleus and nucleoli. They show a plentiful and xanthomatous cytoplasm, with abundant intracytoplasmic pink secretions characteristically. It may be mistaken with low grade adenocarcinomas, and it is essential to differentiate it from the clear cell prostatic adenocarcinoma, prostatic adenosis, and even from benign prostatic hyperplasia. It usually has an intermediate grade, with a Gleason score greater than 4.

journal_name

Arch Esp Urol

authors

Llarena Ibarguren R,Lecumberri Castaños D,Padilla Nieva J,Crespo Atín V,Martín Bazaco J,Azurmendi Sastre V,Eizaguirre Zarza B,Pertusa Peña C

subject

Has Abstract

pub_date

2003-09-01 00:00:00

pages

833-5

issue

7

eissn

0004-0614

issn

1576-8260

journal_volume

56

pub_type

杂志文章,评审
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    doi:

    authors: Maganto Pavón E

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    doi:

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    doi:

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    doi:

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    doi:

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    doi:

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    doi:

    authors: del Rosario Medina J,Chesa Ponce N,Artiles Hernández JL,Betancort de León R

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  • [Treatment of urethral stenosis by self expandable endourethral prosthesis. Long-term results].

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    doi:

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    pub_type: 杂志文章,评审

    doi:

    authors: Asensio Lahoz LA,Sandoval González F,Abaitua Bilbao J,Palazuelos CM,del Valle Schaan JI,García Montesinos M,de La Torriente Oria JI,García de Tuñon A,Lanzas Prieto JM

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  • [Congenital bladder diverticulum as a cause of acute urinary retention].

    abstract::A case of acute urinary retention secondary to a giant bladder diverticulum in a 23-year-old patient is described. Its etiopathogenesis is briefly discussed, highlighting its congenital origin which, in our view, must be based on the histological examination of the specimen. ...

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    authors: Porras V,Pascual JI,Mateos J,Almajano C

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    pub_type: 共识发展会议,杂志文章

    doi:

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    doi:

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  • [Early calculogenesis caused by ureolytic infection of the double-J ureteral catheter].

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    doi:

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