Clinicopathological pattern of cranial unifocal Langerhans cell histiocytosis: A study at medical college hospital

Author:

Bhat Salma1,Nazir Parvez2,Bashir Humaira1,Reshi Ruby1,Sheikh Sheema1,Wani Rohi1

Affiliation:

1. Department of Pathology, Government Medical College, Srinagar, Jammu and Kashmir, India

2. Department of Radiodiagnosis, Real Scan Imaging and Diagnostic Centre, Srinagar, Jammu and Kashmir, India

Abstract

Abstract Background: Eosinophilic granuloma (EG) of bone refers to a generally benign form of Langerhans cell histiocytosis localized to the bone. Patients may present with a solitary lesion (monostotic) or multiple sites of involvement (polyostotic). Materials and Methods: This study was done to evaluate the clinicopathological pattern of 6 cases of EGs of the skull diagnosed at a tertiary care hospital. All patients of EG were included with the help of medical records over a 5-year period that is, November 2009 to November 2014. They all had been preoperatively evaluated by skull X-ray and computed tomography. To rule out a multifocal disease scintigraphy was performed in all cases preoperatively. Surgical excision was performed, and EG was diagnosed on histopathology and immunohistochemistry. Results: There was a male predominance. Parietal bone was the most common affected bone. Total excision of the lesion was performed in all cases. No patient received postoperative radiotherapy. The follow-up period ranged from 6 months to 3 years. No tumor recurrence was noted. Conclusion: With an unknown etiology, nonspecific clinical and radiological findings with diagnosis possible only on histopathological examination, EG needs to be considered in the differential diagnosis as a skull mass, especially in children.

Publisher

Georg Thieme Verlag KG

Subject

Oncology,Pediatrics, Perinatology and Child Health

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