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Granular cell tumor: a clinicopathological study

R Naik1, A S Kamath

  • 1Department of Pathology, Kasturba Medical College, Mangalore.

Indian Journal of Pathology & Microbiology
|July 1, 1993
PubMed
Summary
This summary is machine-generated.

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Granular cell tumors are uncommon neoplasms with uncertain origins. This study analyzed 19 cases, noting a predilection for females aged 30-50 and rare occurrences in sites like the cecum.

Area of Science:

  • Oncology
  • Pathology

Background:

  • Granular cell tumors (GCTs) are rare neoplasms with debated histogenesis.
  • Their occurrence in specific demographics and rare anatomical locations warrants further investigation.

Purpose of the Study:

  • To analyze the clinicopathological features of 19 granular cell tumor cases.
  • To highlight the occurrence of GCT in rare sites, specifically the cecum.

Main Methods:

  • Retrospective analysis of 19 histopathologically confirmed granular cell tumor cases.
  • Review of patient demographics, tumor location, and clinical presentation.

Main Results:

  • The majority of GCTs were observed in females between the third and fifth decades of life.
  • The study documented rare cases of GCT in the cecum, with only two prior reports globally.

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  • Analysis included typical and rare presentations of GCT.

    • Conclusions:

    • Granular cell tumors predominantly affect middle-aged females.
    • The cecum represents an exceptionally rare site for GCT, underscoring the need for awareness and further research into GCT origins and behavior.