Nodular fasciitis: A pseudomalignant clonal neoplasm characterized by USP gene rearrangements and spontaneous regression
نویسندگان
چکیده
منابع مشابه
Spontaneous regression and recurrence in a case of nodular fasciitis.
Sir. Nodular fasciitis is a sporadic tumor that results from a benign proliferation of myofibroblasts in soft tissues. It presents clinically as a rapidly-growing firm nodule, most often localized in the subcutaneous tissue (1). While it may arise in any part ofthe body, there is a predilection for the upper extremities, especially the forearms (1-3). Nodular fasciitis occurs most commonly in y...
متن کاملNodular Fasciitis
odular fasciitis, also known as infiltrative or pseudosarcomatous fasciitis, is a benign soft tissue tumor of fibroblastic/myofibroblastic differentiation that was first described in 1955 by Konwaler et al.1 The lesion often comes to clinical attention when a patient presents with a rapidly growing, occasionally painful, palpable soft tissue mass.2,3 Although benign and self-limited, nodular fa...
متن کاملNodular Fasciitis of the Auricle: A Case Report
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...
متن کاملNodular fasciitis: a diagnostic dilemma.
A 65 year old man presented with a right upper cervical mass. A diagnosis of pleomorphic adenoma was reported on fine needle aspiration cytology (FNAC). CT scan however reported an intramuscular sternocleidomastoid swelling. The tumor was excised and a diagnosis of nodular fasciitis was made. It is important to be aware of this diagnosis and that FNAC reports may mimic that of a pleomorphic ade...
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ژورنال
عنوان ژورنال: International Journal of Case Reports and Images
سال: 2017
ISSN: 0976-3198
DOI: 10.5348/ijcri-201713-cr-10752