Publication:
Appendiceal involvement in a patient with Gaucher disease

dc.contributor.authorKocic, Marija (57192209334)
dc.contributor.authorDjuricic, Slavisa M (6603108728)
dc.contributor.authorDjordjevic, Maja (7102319301)
dc.contributor.authorSavic, Djordje (15078056700)
dc.contributor.authorKecman, Bozica (23034935300)
dc.contributor.authorSarajlija, Adrijan (26027638400)
dc.date.accessioned2025-07-02T12:16:09Z
dc.date.available2025-07-02T12:16:09Z
dc.date.issued2018
dc.description.abstractAlmost any anatomical compartment may be involved in Gaucher disease (GD). Abdominal lymphadenopathy occurred during enzyme replacement therapy in more than a dozen children with GD so far. A fourteen-year-old boy from Serbia developed clinical signs of acute appendicitis six years after the onset of GD type 3 related abdominal lymphadenopathy. Ultrasound examination showed diffuse thickening of the intestinal wall in the ileocoecal region with periappendicular infiltration. An appendectomy was performed four months after conservative treatment with antibiotics. Histopathology revealed macrophages with cytological characteristics of Gaucher cells densely crammed in mesoappendiceal adipose tissue. Also the multifocal replacement of subserosal tissue by Gaucher cells and their infiltration to a variable depth of muscularis propria of the appendix were verified. Frank infiltration of the vermiform appendix with Gaucher cells represents a novel observation in a wide spectrum of manifestations reported in GD. A possible causative relationship of this infiltration with appendicitis is considered. © 2016 Elsevier Inc.
dc.identifier.urihttps://doi.org/10.1016/j.bcmd.2016.09.002
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85000919293&doi=10.1016%2fj.bcmd.2016.09.002&partnerID=40&md5=37255dc7bd491c08ef3942bba7b2f3f0
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/13014
dc.subjectAbdominal lymphadenopathy
dc.subjectAppendicitis
dc.subjectAppendix
dc.subjectGaucher disease
dc.titleAppendiceal involvement in a patient with Gaucher disease
dspace.entity.typePublication

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