Results 41 to 50 of about 1,034 (137)

Pigmented clear cell sarcoma of soft tissue: an important diagnostic mimic [PDF]

, 2022
Clear cell sarcoma of soft tissue (CCSST) is a rare and aggressive soft tissue tumour associated with tendons and aponeuroses of the lower extremities.
De Noon, Solange, Flanagan, Adrienne M, Mendes, Bernardo Souza   +2 more
core  

Histiocyte‐rich ROS1‐rearranged inflammatory myofibroblastic tumour of the trachea: A rare neoplasm presenting with asthma‐like symptoms

Respirology Case Reports, Volume 12, Issue 12, December 2024.
A flow volume loop demonstrated classical upper airway obstruction pattern. Abstract Inflammatory myofibroblastic tumour is a rare tumour. We present an atypical case of Inflammatory myofibroblastic tumour which was trachea in location, histocyte rich and ROS1 rearranged.
Chin Tong Kwok, Jason Cheuk Ho Tsang, Mary Lam, Sandy Sze Ki Ho, Chi Sum Yuen, Yiu Cheong Yeung   +5 more
wiley   +1 more source

Manifestação Incomum de uma Entidade Rara: Doença de Erdheim-Chester [PDF]

, 2019
A 69-year-old woman presented with sudden left hemiparesis. Computed tomography (CT) scan excluded acute brain injuries. Patient was admitted with acute ischemic stroke of right hemisphere. There was full recovery within 24 hours and etiologic studies
Achega, M, Aldomiro, F, Martins, N, Rodrigues, A   +3 more
core   +1 more source

A Rare Xanthogranulomatous Oophoritis Presenting as Ovarian Cancer [PDF]

, 2012
Xanthogranulomatous inflammation is an uncommon form of chronic inflammation that is destructive to affected organs; it is characterized by the presence of lipid-filled macrophages with admixed lymphocytes, plasma cells, and neutrophils. Only a few cases
Bafna, UD, Devi, UK, Gouda, G, Kalloli M, M, Mukherjee, G, Rathod, PS   +5 more
core  

Multinucleated Giant Cells Polymorphism in Epulis [PDF]

, 2015
In the present study we investigated multinucleated giant cells (MGCs) presence, density and morphology in epulis. Histopathological examination performed on specimens excised from two patients and stained using Goldner’s trichrome method revealed MGCs
Boșca, Adina Bianca, Constantin, Anne Marie, Ilea, Aranka, Miclăuș, Viorel, Rațiu, Cristian, Rus, Vasile, Ruxanda, Flavia, Șovrea, Alina Simona   +7 more
core   +2 more sources

Erdheim–Chester disease: An elusive diagnosis in a 50‐year‐old Ethiopian man presenting with diffuse sclerotic bone lesion

Clinical Case Reports, Volume 12, Issue 9, September 2024.
Key Clinical Message Diagnosis of Erdheim–Chester disease (ECD) requires the clinician to be familiar with its various manifestations, classic radiologic and histologic features. This case highlights the significance of considering ECD in any patient presenting with bone pain and symmetric osteosclerosis of long bones of extremities to allow for early ...
Semir Abdi Usmael, Addisu Alemu Gebrehiywot, Ashenafi Lemma Bekele, Solomon Bishaw Yezengaw, Tekalign Tsegaye Tefera, Hunduma Bikila Bote, Kalkidan Abera Shibeshi, Anteneh Belachew Fantaye   +7 more
wiley   +1 more source

Lingual juvenile xanthogranuloma in a woman: a case report [PDF]

, 2011
Introduction Juvenile xanthogranuloma is a rare non-Langerhans cell histiocytosis that usually occurs during infancy and early childhood. The presence of single or multiple raised cutaneous lesions characterize this self-healing disorder.
A Consolaro, A Hernandez-Martin, AC Crocker, Alessandro Villa, C Flaitz, DG Stover, EB Helwig, FE Senear, Francesco Villa, HG Adamson, OP Sangueza, S Kawashiri, SB Webster, SJ Satow, Umberto Mariani   +14 more
core   +3 more sources

Necrobiotic xanthogranuloma: A case report of successful treatment with intravenous immunoglobulins

JEADV Clinical Practice, Volume 3, Issue 4, Page 1248-1252, September 2024.
Abstract Necrobiotic xanthogranuloma (NXG) is a rare non‐Langerhans cell histiocytosis associated with paraproteinemia. Skin lesions of NXG are difficult to treat and various therapies have been evaluated with inconsistent results. A therapeutic standard has not been established.
Julia K. Winkler, Holger A. Haenssle, Jochen Hoffmann, Ferdinand Toberer, Alexander H. Enk   +4 more
wiley   +1 more source

Pilomatricoma in the infraorbital region

Clinical Case Reports, Volume 12, Issue 8, August 2024.
Key Clinical Message Pilomatricoma, a rare benign skin tumor arising from hair follicle matrix cells, warrants consideration in the evaluation of subcutaneous nodules or masses, especially when presenting as painless and firm lesions. Accurate diagnosis hinges on histopathological examination, underscoring the significance of clinician vigilance and ...
Dilasha Dhungel, Varun Rastogi, Sandhya Chaurasia, Nisha Maddheshiya   +3 more
wiley   +1 more source

Cutaneous crystal storing histiocytosis: A case series with review of literature

Journal of Cutaneous Pathology, Volume 51, Issue 7, Page 506-512, July 2024.
Abstract Crystal‐storing histiocytosis (CSH) is a rare condition in which crystals accumulate in the cytoplasm of histiocytes and is usually associated with a lymphoplasmacytic neoplasm. Cutaneous CSH is extraordinarily rare and limited to case reports in the literature. We report two cases of this disease with cutaneous involvement.
Haya A. Homsi, Calvin Knapp III, Shruti Agrawal, Shweta Bhavsar, Jennifer S. Ko, Steven D. Billings, Shira Ronen   +6 more
wiley   +1 more source