Spitz tumour with ALK rearrangement: a case report and literature review

Spitz tumour with ALK rearrangement is a recently described entity and a rare tumour. The incidence of Spitz tumour was estimated at 3.63 per 100,000 persons in American paediatric population; while there is no data in Asian population. Here we reported a case of an eleven-year-old Asian boy who pre...

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Main Authors: Lai, Shau-Kong, Bakrin, Ikmal Hisyam, Abd Rauf,, Nurhafidzah, Abdul Raub, Sayyidi Hamzi
Format: Article
Language:English
Published: Malaysian Society of Pathologists 2024
Online Access:http://psasir.upm.edu.my/id/eprint/113566/1/113566.pdf
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author Lai, Shau-Kong
Bakrin, Ikmal Hisyam
Abd Rauf,, Nurhafidzah
Abdul Raub, Sayyidi Hamzi
author_facet Lai, Shau-Kong
Bakrin, Ikmal Hisyam
Abd Rauf,, Nurhafidzah
Abdul Raub, Sayyidi Hamzi
author_sort Lai, Shau-Kong
collection UPM
description Spitz tumour with ALK rearrangement is a recently described entity and a rare tumour. The incidence of Spitz tumour was estimated at 3.63 per 100,000 persons in American paediatric population; while there is no data in Asian population. Here we reported a case of an eleven-year-old Asian boy who presented with a left shin nodule of two months’ duration. The skin biopsy revealed a Spitz tumour with predominantly spindle cell morphology arranged in fascicles, vertically orientated nests and radial growth pattern. Junctional component, melanin pigment or Kamino bodies were not identified. Immunohistochemical study displayed homogenous cytoplasmic staining for ALK. Fluorescence in-situ hybridisation (FISH) analysis confirmed ALK rearrangement. Review of the literatures demonstrated that positive ALK immunohistochemistry may not correlate with ALK rearrangement. ALK-rearranged Spitz tumour confirmed with FISH analysis favour clinically benign behaviour despite atypical histomorphology or positive sentinel lymph node. Therefore, correlation of histomorphology, immunohistochemical stain and molecular study are important for the definitive diagnosis of this entity.
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spelling upm.eprints-1135662024-11-26T04:30:09Z http://psasir.upm.edu.my/id/eprint/113566/ Spitz tumour with ALK rearrangement: a case report and literature review Lai, Shau-Kong Bakrin, Ikmal Hisyam Abd Rauf,, Nurhafidzah Abdul Raub, Sayyidi Hamzi Spitz tumour with ALK rearrangement is a recently described entity and a rare tumour. The incidence of Spitz tumour was estimated at 3.63 per 100,000 persons in American paediatric population; while there is no data in Asian population. Here we reported a case of an eleven-year-old Asian boy who presented with a left shin nodule of two months’ duration. The skin biopsy revealed a Spitz tumour with predominantly spindle cell morphology arranged in fascicles, vertically orientated nests and radial growth pattern. Junctional component, melanin pigment or Kamino bodies were not identified. Immunohistochemical study displayed homogenous cytoplasmic staining for ALK. Fluorescence in-situ hybridisation (FISH) analysis confirmed ALK rearrangement. Review of the literatures demonstrated that positive ALK immunohistochemistry may not correlate with ALK rearrangement. ALK-rearranged Spitz tumour confirmed with FISH analysis favour clinically benign behaviour despite atypical histomorphology or positive sentinel lymph node. Therefore, correlation of histomorphology, immunohistochemical stain and molecular study are important for the definitive diagnosis of this entity. Malaysian Society of Pathologists 2024 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/113566/1/113566.pdf Lai, Shau-Kong and Bakrin, Ikmal Hisyam and Abd Rauf,, Nurhafidzah and Abdul Raub, Sayyidi Hamzi (2024) Spitz tumour with ALK rearrangement: a case report and literature review. Malaysian Journal of Pathology, 46 (1). pp. 103-108. ISSN 0126-8635 https://www.mjpath.org.my/2024/v46n1/spitz-tumour.pdf
spellingShingle Lai, Shau-Kong
Bakrin, Ikmal Hisyam
Abd Rauf,, Nurhafidzah
Abdul Raub, Sayyidi Hamzi
Spitz tumour with ALK rearrangement: a case report and literature review
title Spitz tumour with ALK rearrangement: a case report and literature review
title_full Spitz tumour with ALK rearrangement: a case report and literature review
title_fullStr Spitz tumour with ALK rearrangement: a case report and literature review
title_full_unstemmed Spitz tumour with ALK rearrangement: a case report and literature review
title_short Spitz tumour with ALK rearrangement: a case report and literature review
title_sort spitz tumour with alk rearrangement a case report and literature review
url http://psasir.upm.edu.my/id/eprint/113566/1/113566.pdf
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