Short-Spindled Cell Haemangioblastoma with CD34 Expression: New Histopathological Variant or Just a Stochastic Cytological Singularity?

Haemangioblastomas are neoplasms of uncertain histogenesis with cellular and reticular variants advocated in current lore. Herein we describe an intriguing cerebellar specimen with unusual traits including spindle cell morphology and CD34 positivity. A thirty-nine-year old man had an infratentorial...

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Main Authors: Miguel Fdo. Salazar, Paola Andrea Escalante Abril, María Verónica Velasco Vales, Celene Martínez Ruiz, Erick Gómez Apo, Laura G. Chávez Macías
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Case Reports in Pathology
Online Access:http://dx.doi.org/10.1155/2016/6749590
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author Miguel Fdo. Salazar
Paola Andrea Escalante Abril
María Verónica Velasco Vales
Celene Martínez Ruiz
Erick Gómez Apo
Laura G. Chávez Macías
author_facet Miguel Fdo. Salazar
Paola Andrea Escalante Abril
María Verónica Velasco Vales
Celene Martínez Ruiz
Erick Gómez Apo
Laura G. Chávez Macías
author_sort Miguel Fdo. Salazar
collection DOAJ
description Haemangioblastomas are neoplasms of uncertain histogenesis with cellular and reticular variants advocated in current lore. Herein we describe an intriguing cerebellar specimen with unusual traits including spindle cell morphology and CD34 positivity. A thirty-nine-year old man had an infratentorial tumour discovered incidentally and resected three times. In all the instances, histopathological diagnosis was haemangioblastoma; nonetheless, he had neither physical stigmata nor family history of von Hippel-Lindau disease. By histology, the lesion was composed of areas of conventional stromal cells admixed with territories populated by short-spindled cells packed in lobules, sometimes giving the appearance of gomitoli. Immunoperoxidase-coupled reactions confirmed the expression of inhibin A, neuron-specific enolase (NSE), PS100, and CD57 but also revealed focal immunolabeling for CD34, CD99, and FXIIIa. This case highlights the potential phenotypical diversity that can be found within these neoplasms. Rather than uncertain histogenesis, it may in fact reflect multiple lines of differentiation—histomimesis—prone to adopt unusual morpho- and immunophenotypes in a subset of haemangioblastomas.
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spelling doaj-art-ee4160cb027d4367b63b38566890780c2025-08-20T03:20:43ZengWileyCase Reports in Pathology2090-67812090-679X2016-01-01201610.1155/2016/67495906749590Short-Spindled Cell Haemangioblastoma with CD34 Expression: New Histopathological Variant or Just a Stochastic Cytological Singularity?Miguel Fdo. Salazar0Paola Andrea Escalante Abril1María Verónica Velasco Vales2Celene Martínez Ruiz3Erick Gómez Apo4Laura G. Chávez Macías5Pathology Unit, Neuropathology Service, Mexico General Hospital, 06726 Cuauhtémoc, DF, MexicoPathology Unit, Neuropathology Service, Mexico General Hospital, 06726 Cuauhtémoc, DF, MexicoPathology Unit, Neuropathology Service, Mexico General Hospital, 06726 Cuauhtémoc, DF, MexicoPathology Unit, Neuropathology Service, Mexico General Hospital, 06726 Cuauhtémoc, DF, MexicoPathology Unit, Neuropathology Service, Mexico General Hospital, 06726 Cuauhtémoc, DF, MexicoPathology Unit, Neuropathology Service, Mexico General Hospital, 06726 Cuauhtémoc, DF, MexicoHaemangioblastomas are neoplasms of uncertain histogenesis with cellular and reticular variants advocated in current lore. Herein we describe an intriguing cerebellar specimen with unusual traits including spindle cell morphology and CD34 positivity. A thirty-nine-year old man had an infratentorial tumour discovered incidentally and resected three times. In all the instances, histopathological diagnosis was haemangioblastoma; nonetheless, he had neither physical stigmata nor family history of von Hippel-Lindau disease. By histology, the lesion was composed of areas of conventional stromal cells admixed with territories populated by short-spindled cells packed in lobules, sometimes giving the appearance of gomitoli. Immunoperoxidase-coupled reactions confirmed the expression of inhibin A, neuron-specific enolase (NSE), PS100, and CD57 but also revealed focal immunolabeling for CD34, CD99, and FXIIIa. This case highlights the potential phenotypical diversity that can be found within these neoplasms. Rather than uncertain histogenesis, it may in fact reflect multiple lines of differentiation—histomimesis—prone to adopt unusual morpho- and immunophenotypes in a subset of haemangioblastomas.http://dx.doi.org/10.1155/2016/6749590
spellingShingle Miguel Fdo. Salazar
Paola Andrea Escalante Abril
María Verónica Velasco Vales
Celene Martínez Ruiz
Erick Gómez Apo
Laura G. Chávez Macías
Short-Spindled Cell Haemangioblastoma with CD34 Expression: New Histopathological Variant or Just a Stochastic Cytological Singularity?
Case Reports in Pathology
title Short-Spindled Cell Haemangioblastoma with CD34 Expression: New Histopathological Variant or Just a Stochastic Cytological Singularity?
title_full Short-Spindled Cell Haemangioblastoma with CD34 Expression: New Histopathological Variant or Just a Stochastic Cytological Singularity?
title_fullStr Short-Spindled Cell Haemangioblastoma with CD34 Expression: New Histopathological Variant or Just a Stochastic Cytological Singularity?
title_full_unstemmed Short-Spindled Cell Haemangioblastoma with CD34 Expression: New Histopathological Variant or Just a Stochastic Cytological Singularity?
title_short Short-Spindled Cell Haemangioblastoma with CD34 Expression: New Histopathological Variant or Just a Stochastic Cytological Singularity?
title_sort short spindled cell haemangioblastoma with cd34 expression new histopathological variant or just a stochastic cytological singularity
url http://dx.doi.org/10.1155/2016/6749590
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