Loading…

IgG4-related disease of the paratestis in a patient with Wells syndrome: a case report

We report a case of a 33-year-old man who presented with immunoglobulin (Ig)G4-related disease (IgG4-RD) forming a pseudotumor in the left paratesticular region during oral administration of corticosteroid for Wells syndrome, which involves cellulitis with eosinophilia. The patient was introduced to...

Full description

Saved in:
Bibliographic Details
Published in:Diagnostic pathology 2014-12, Vol.9 (1), p.225-225, Article 225
Main Authors: Karashima, Takashi, Taniguchi, Yoshinori, Shimamoto, Tsutomu, Nao, Tomoya, Nishikawa, Hiroshi, Fukata, Satoshi, Kamada, Masayuki, Inoue, Keiji, Oko, Kentaro, Nakajima, Hideki, Sano, Shigetoshi, Matsumoto, Manabu, Kuroda, Naoto, Kamei, Yoshihiro, Shuin, Taro
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:We report a case of a 33-year-old man who presented with immunoglobulin (Ig)G4-related disease (IgG4-RD) forming a pseudotumor in the left paratesticular region during oral administration of corticosteroid for Wells syndrome, which involves cellulitis with eosinophilia. The patient was introduced to our institution from a private hospital with a 3-month history of asymptomatic left scrotal mass. A 5-cm diameter nodule was palpable in the left scrotum. Tumor lesion in the left paratestis involving the epididymis and spermatic cord was observed on computed tomography and magnetic resonance imaging. Blood testing showed no abnormalities other than a minimal increase in C-reactive protein levels. Urine examination likewise revealed no significant findings. Left radical orchidectomy was performed under a diagnosis of left paratesticular neoplasm suspected as malignant tumor. The tumor was pathologically identified as IgG4-RD of the left paratestis involving the epididymis and spermatic cord. We present a first description of IgG4-RD in a patient with Wells syndrome and the ninth case of IgG4-RD in a scrotal organ, and discuss this very rare entity with reference to the literature. The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_225.
ISSN:1746-1596
1746-1596
DOI:10.1186/s13000-014-0225-5