Publication:
A Rare Cause of Intestinal Obstruction: Neonatal Gastrointestinal Stromal Tumor

Loading...
Thumbnail Image

relationships.isOrgUnitOf

Program

relationships.isAuthorOf

Author

KOKU, NAİM

DEMİRCİ, MUSTAFA

KARAKOK, METİN

CITAK, ELVAN CAGLAR

Advisor

Language

Publisher

Journal Title

Journal ISSN

Volume Title

Abstract

Gastrointestinal stromal tumors (GISTs) are rare in the childhood period. The authors reported a case who was admitted to the neonatal intensive care unit (NICU) on a suspicion of intestinal obstruction. She was operated and a mass in a size of 6 xx 4.5 xx 4 cm was resected from the ileum. Histologic and immunohistochemical studies showed a GIST. CD34, small muscle actin (SMA), and desmin were positive. The baby was discharged on the 13th day after operation.</.

Description

Source

Keywords

Keywords

Citation

TANYERİ B., -A Rare Cause of Intestinal Obstruction: Neonatal Gastrointestinal Stromal Tumor-, Pediatric Hematology And Oncology, 2011

Endorsement

Review

Supplemented By

Referenced By

4

Views

0

Downloads


Sustainable Development Goals