Results 21 to 30 of about 207,165 (127)
Subcutaneous Dermatofibroma: A Rare Case Report with Review of Literature [PDF]
Journal of Clinical and Diagnostic Research, 2014 A purely Sub-cutaneous benign fibrous histiocytoma (BFH; dermatofibroma) is rarely reported, as it is usually a dermally located mesenchymal tumour and in absence of supportive immunohistochemical (IHC) studies, it is often misdiagnosed.
Harjot Kaur +4 more
doaj +1 more source
PU.1 is a useful nuclear marker to distinguish between histiocytosis and histiocyte‐rich tumours
Histopathology, Volume 83, Issue 2, Page 320-325, August 2023., 2023 Aims The aim was to test the expression of PU.1 on different types of histiocytoses and to test the utility of PU.1 in confirming or excluding a histiocytic origin in tumour samples with suspicion of histiocytosis. Methods and Results We analysed 66 biopsies of nonmalignant histiocytoses represented by Langerhans‐cell histiocytosis (n = 13), Erdheim ...
Irena Antonia Ungureanu +5 more
wiley +1 more source
Syringomatous adenoma of the nipple: A case series and systematic review
Clinical Case Reports, Volume 11, Issue 6, June 2023., 2023 Demonstration of keratin cysts giving the characteristic teardrop or comma‐like shape. Key Clinical Message SAN should be considered in the setting of nipple discharge or morphology changes with typical histological findings. There are limited published cases of SAN, and workup of this pathology is still not clear to date.
Sean K. Park +3 more
wiley +1 more source
A Rare Case of Pleomorphic Fibroma Associated with Li-Fraumeni Syndrome
Graduate Medical Education Research Journal, 2023 Mentor: Dominick DiMaio. Program: Pathology Type: Case Report Background: Li-Fraumeni syndrome is a germline mutation in the TP53 gene which causes an increased risk of various neoplasms like ovarian, colorectal, soft tissue, and hematopoietic tumors ...
Samir Atiya, Dominick DiMaio
doaj +1 more source
Dermatofibroma-like granular cell tumour: a potential diagnostic pitfall [PDF]
, 2016 Dermatofibroma-like granular cell tumour (GCT) is a rare entity, with only two cases having been described so far. We report another case in a 62-year-old woman, discuss histopathological features, and review other tumours in which granular changes have ...
Ales Ryska +2 more
core +1 more source
Cholesterotic Fibrous Histiocytoma in a Patient with Metabolic Syndrome
Case Reports in Dermatology, 2017 Among the many variants of dermatofibroma, dermatofibroma with cholesterol cleft (cholesterotic fibrous histiocytoma) is extremely rare. Here, we describe the case of a 50-year-old male patient with a cholesterotic fibrous histiocytoma on his left lower ...
Masatoshi Deguchi, Setsuya Aiba
doaj +1 more source
Carcinoma basocelular superficial sobre dermatofibroma [PDF]
, 1996 Se presenta el caso de una mujer, de 53 años de edad, a quien se le diagnosticó un dermatofibroma. Posterior a la resección total, el estudio histopatológico mostró un dermatofibroma típico sobre el cual se asienta un carcinoma basocelular
Arévalo Ramírez, Néstor Fernando
core +1 more source
Emergence of solitary juvenile xanthogranuloma on the corneoscleral limbus
Journal of Clinical Ophthalmology and Research, 2018 Juvenile xanthogranuloma (JXG) is the most frequent form of non-Langerhans histiocytosis, a rare benign inflammatory skin disorder. Eye involvement is the most frequent extracutaneous manifestation of the disease.
Raul Alfaro-Rangel +2 more
doaj +1 more source
A case of atrophic dermatofibroma
, 2021 Dermatofibromas are benign tumors caused by fibroblasts and histiocytes, which are quite common in middle-aged adults. It is characterized by hard, single or multiple, papule, plaque or nodul-shaped lesions that are localized to the lower extremity. Many
BAYRAMGÜRLER, DİLEK +7 more
core +1 more source
, 2013 Dermatofibroma is a benign fibrohistiocytic tumor, common and easily diagnosed when classical clinicopathologic features are present. The atrophic variant of dermatofibroma is of uncertain origin.
Mota,Amanda Nascimento C. de Macedo +3 more
core +1 more source