INTRODUCTION Lipofibromatosis is a rare fibro-fatty tumour with a predilection to involve distal extremities. It has only recently been described as a distinctive clinicopathologic entity, and subsequently only a few cases have been published in the literature. To address the clinicopathologic significance of this rare entity, we here describe a case of lipofibromatosis occurring on the left th...

David Brown, Olivier Sarbach, Erik Schnetter, Manuel Tiglio, Peter Diener, Ian Hawke, and Denis Pollney Department of Physics, North Carolina State University, Raleigh, North Carolina 27695, USA Instituto de Fı́sica y Matemáticas, Universidad Michoacana de San Nicolás de Hidalgo, Morelia, Michoacán, México Center for Computation & Technology, Louisiana State University, Baton Rouge, Louisiana, U...

Introduction: Nodular fasciitis is described as a benign reactive proliferation of myofibroblasts. Due to its rapid-growing nature, a precise clinical diagnosis is difficult and the condition is frequently misdiagnosed as malignant lesions.   Case Report: In this study, we present the case of a young woman with an auricular nodular fasciitis as an example of one of the rarest sites of this tumo...

Background Scrotal leiomyosarcomas are extremely rare and hence the biological behaviour of these rare tumours may not be known by most medical practitioners. To the knowledge of the authors about 37 cases of leiomyosarcoma of scrotum have so far been reported. Aims To report a case of leiomyosarcoma of scrotum To review the literature on leiomyosarcomas of scrotum Case Report A 66-years-old ma...

UNLABELLED The aim of this retrospective study was to assess whether open surgical excision is required following a B3 diagnosis on 11-gauge vacuum-assisted core biopsy (VACB) of radiologically indeterminate breast lesions. PATIENTS AND METHODS Twenty-four women with a histological diagnosis of the B3 category on VACB of radiologically indeterminate breast lesions were identified over a 3-yea...

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Juvenile ossifying fibroma (JOF) is a rare, benign, locally aggressive entity of the extragnathic craniofacial bones with a high tendency towards recurrence. Two distinctive microscopic patterns of juvenile ossifying fibroma have been described: a trabecular juvenile ossifying fibroma (TrJOF) and a psammomatoid juvenile ossifying fibroma (PJOF). Psammomatoid variant is predominantly a craniofac...