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Hemophagocytic lymphohistiocytosis associated with Epstein-Barr virus infection: case report and literature review.
Bahabri, Saeed; Al Rikabi, Ammar C; Alshammari, Amjad O; Alturkestany, Sara I.
Afiliación
  • Bahabri S; Department of Histopathology and Cytology, King Khalid University Hospital, King Saud University, Kingdom of Saudi Arabia.
  • Al Rikabi AC; Department of Histopathology and Cytology, King Khalid University Hospital, King Saud University, Kingdom of Saudi Arabia.
  • Alshammari AO; Department of Histopathology and Cytology, King Khalid University Hospital, King Saud University, Kingdom of Saudi Arabia.
  • Alturkestany SI; Taibah University, Madinah, Kingdom of Saudi Arabia.
J Surg Case Rep ; 2019(6): rjy096, 2019 Jun.
Article en En | MEDLINE | ID: mdl-31275547
ABSTRACT
Hemophagocytic lymphohistiocytosis (HLH) is rare and life threatening syndrome. There are only a few reported cases of HLH with GI symptoms. We describe the case of an 18 months old boy who presented with a history of fever for 40 days, abdominal distention and hepatosplenomegaly. Abdominal x-ray showed a pneumoperitoneum. Urgent laparotomy was done which revealed an isolated cecal perforation. The histopathological findings in the subsequent resected bowel was HLH with evidence of positive EBV Barr infection.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies / Systematic_reviews Idioma: En Revista: J Surg Case Rep Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies / Systematic_reviews Idioma: En Revista: J Surg Case Rep Año: 2019 Tipo del documento: Article