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http://dx.doi.org/10.1111/ans.17570 | DOI Listing |
J Surg Case Rep
May 2024
Plastic Surgery Department, Hospital Clinico Universitario de Santiago de Compostela, Rua Choupana s/n, Santiago de Compostela 15706, Spain.
Pleomorphic lipomas are infrequent soft tissue tumours with pseudosarcomatous behaviour. Their polymorphism provides them certain characteristics that may resemble malignancy, which may mislead the initial diagnosis. The presented case report is a 45-year-old man with a giant growing tumour on the left cervicoscapular region initially categorised as a liposarcoma by magnetic resonance with a final confirmed diagnosis of pleomorphic lipoma after the surgical resection and the examination of the pathologist.
View Article and Find Full Text PDFPathol Oncol Res
February 2023
Department of Surgical Pathology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
The intramuscular subtype of nodular fasciitis (NF) is rare with lesions normally not more than 2 cm in size and characterized by pseudosarcomatous morphology. We report a case of a 27-year-old man with a large-size intramuscular NF. The patient came for treatment complaining of an increasingly enlarged mass in the left upper arm for 4 months.
View Article and Find Full Text PDFANZ J Surg
November 2022
HPB/Transplant Unit, Department of Surgery (Austin Precinct), The University of Melbourne, Austin Health, Melbourne, Victoria, Australia.
Pleomorphic lipoma is an uncommon, pseudosarcomatous lesion. It is characterized by the pleomorphic appearance on cytology and histology, follows a benign course, with a low rate of recurrence after complete excision, and has no risk of metastasis. Here, we describe a case of pleomorphic lipoma/spindle cell lipoma in a 41-year-old man who presented with a slow-growing mass on the inner aspect of the left thigh.
View Article and Find Full Text PDFIndian J Dent Res
November 2019
Department of Oral Pathology and Microbiology, Government Dental College, Kozhikode, Kerala, India.
Proliferative fasciitis is a pseudo-sarcomatous myofibroblastic proliferation characterized by the presence of unusual giant cells resembling ganglion cells, which usually occurs in the adult population with a mean age of 54 years. It usually affects the upper extremities and is rare in head and neck region with only 11 cases described in the literature so far. Because of rapid growth and histological similarity to various malignant tumors such as rhabdomyosarcoma, recognition of this benign condition is a matter of utmost importance when a pathologist is concerned.
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