𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Multiple granular cell tumor: A case report and review of the literature

✍ Scribed by Brett Vean Curtis; Thomas C. Calcaterra; Walter F. Coulson

Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
152 KB
Volume
19
Category
Article
ISSN
1043-3074

No coin nor oath required. For personal study only.

✦ Synopsis

Background. Granular cell tumor was first described by Abrikossoff in 1926. It is rare and usually presents as a benign solitary lesion. Multifocal and malignant forms are known to occur.

Methods. This presentation illustrates an additional case of granular cell tumor. Clinical and histological features to distinguish malignant and benign forms are presented.

Results. Tumor can develop years after therapy for the primary lesion. Treatment recommendations are presented.

Conclusions. Patients diagnosed with granular cell tumor require close follow-up. Radiographic evaluation for the presence of metastatic disease is necessary if a malignant variant is suspected.

πŸ“œ SIMILAR VOLUMES

Giant cell tumor of the larynx: Case rep
Giant cell tumor of the larynx: Case report and review of the literature
✍ Jochen A. Werner; Dieter Harms; Arwed Beigel πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 332 KB πŸ‘ 1 views

Background: Primary manifestation of a giant cell chondrosarcomas. The primary manifestation of tumor (GCT) in the larynx is exceedingly rare. Until now, only 17 a giant cell tumor (GCT) in the larynx is exceedcases have been reported in the literature. Characterization of a GCT can be difficult par

Aggressive T-cell large granular lymphoc
Aggressive T-cell large granular lymphocyte leukemia: A case report and review of the literature
✍ Todd J. Alekshun; Jianguo Tao; Lubomir Sokol πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 167 KB πŸ‘ 1 views

## Abstract The majority of patients with T‐cell large granular lymphocyte (LGL) leukemia will have an indolent clinical course. Herein, we report a case of an aggressive T‐cell LGL leukemia in a previously healthy 42‐year‐old Caucasian male who presented with acute onset of B‐symptoms, hepatosplen

Paratesticular desmoplastic small round
Paratesticular desmoplastic small round cell tumor: Case report and review of the literature
✍ Roganovich, Jelena; Bisogno, Gianni; Cecchetto, Giovanni; D'Amore, Emanuele S.G. πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 50 KB πŸ‘ 1 views

Desmoplastic small round cell tumor (DSRCT) is a rare neoplasm mainly affecting young males and typically located in the abdomen. Prognosis is generally very poor. We report a rare case of paratesticular DSRCT in a 17-year-old boy, presenting with an isolated left scrotal mass. The patient had an ex