A Rare Abdominal Tumour in a Paediatric Age Group: Pheochromocytoma

Publication:
A Rare Abdominal Tumour in a Paediatric Age Group: Pheochromocytoma

creativeworkseries.issn	ISSN 1990-7974 eISSN 1990-7982
dc.contributor.author	Sah, Rajesh Prasad
dc.contributor.author	Sah, R.G.
dc.contributor.author	Mahmood, Shaukat
dc.date.accessioned	2026-02-09T07:00:54Z
dc.date.available	2026-02-09T07:00:54Z
dc.date.issued	2017
dc.description	Rajesh Prasad Sah Kanti Children Hospital, Maharajgunj, Kathmandu R.G. Sah University of Calgary Shaukat Mahmood King Edward Medical University, Mayo Hospital, Lahore
dc.description.abstract	Abstract: A 10 year boy presented with history of abdominal pain and palpitation. Abdominal ultrasound and CT oriented towards the diagnosis. After preoperative optimization, laparotomy with complete excision of an unusual pheochromocytoma tumour of about 8×10 cm adherent to liver and IVC performed. Histopathology confirmed the diagnosis without evidence of malignancy.
dc.identifier	https://doi.org/10.3126/jnps.v37i1.16885
dc.identifier.uri	https://hdl.handle.net/20.500.14572/4593
dc.language.iso	en_US
dc.publisher	Nepal Paediatric Society (JNPS)
dc.subject	Adrenalectomy
dc.subject	Laparotomy
dc.subject	Pheochromocytoma
dc.title	A Rare Abdominal Tumour in a Paediatric Age Group: Pheochromocytoma
dc.type	Article
dspace.entity.type	Publication
local.article.type	Case Report
oaire.citation.endPage	88
oaire.citation.startPage	86
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