Benign Fibrous Histiocytoma of Gingiva: A Rare Case Report
Contemporary Clinical DentistryFibrous histiocytoma is a benign soft-tissue neoplasm that commonly involves the dermis. It is rare in the oral cavity. This lesion creates a diagnostic dilemma due to its nonspecific clinical appearance and microscopic similarities with other benign ...
Bhavani Nagendra Sangala +5 more
doaj +1 more source
Nonimmune fetal hydrops and lysosomal storage disease: the finding of vacuolated lymphocytes in ascitic fluid in two cases [PDF]
, 2013 Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/102650/1/pd4274 ...
Berman, D. R. +4 more
core +1 more source
A 50‐year‐old man with a 12‐year history of extensive pachymeningeal thickening
Brain Pathology, EarlyView.
Alyssa M. Lee +3 more
wiley +1 more source
Xanthogranuloma of the lacrimal sac as a manifestation of Wegener's granulomatosis [PDF]
, 2007 McGill Univ, Ctr Hlth, Dept Ophthalmol & Pathol, Montreal, PQ H3A 2B4, CanadaHenry C Witelson Ocular Pathol Lab, Montreal, PQ, CanadaUniversidade Federal de São Paulo, Dept Ophthalmol, UNIFESP, EPM, São Paulo, BrazilMcGill Univ, Ctr Hlth, Dept Ophthalmol,
A Al-Kandari +8 more
core +1 more source
International Archives of Otorhinolaryngology, 2014 Introduction Rosai-Dorfman disease (RDD) is a rare histiocytic proliferative disorder of unknown etiology. Usually it presents with massive painless cervical lymph node enlargement.
Rabindra Bhakta Pradhananga +3 more
doaj +1 more source
Eosinophilic fasciitis (Shulman's disease): review and comparative evaluation of seven patients. [PDF]
, 2019 OBJECTIVES: Eosinophilic fasciitis (EF) was described in 1974 by Shulman as a rare fibrosing connective tissue disease of unknown etiology. An undetermined trigger is thought to lead to the degranulation of eosinophils that interact with fibroblasts and
Cimbron, M +3 more
core +1 more source
Histiocytic Sarcoma: Identification of Its Histiocytic Origin Using Immunohistochemistry
Internal Medicine, 2008 We describe a 56-year-old woman with histiocytic sarcoma involving the bone marrow. The neoplastic cells proliferated diffusely and showed occasional erythrophagocytosis. Immunohistochemically, the neoplastic cells were positive for CD68, lysozyme, CD4 and CD163, but negative for B- and T-cell markers, S100 protein and epithelial markers.
Chikamasa, Yoshida, Makoto, Takeuchi
openaire +3 more sources
Necrobiotic xanthogranuloma: A case report of successful treatment with intravenous immunoglobulins
JEADV Clinical PracticeNecrobiotic 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.
Julia K. Winkler +4 more
doaj +1 more source
Gastric crystal-storing histiocytosis without any underlying disorders: Report of a case
Human Pathology: Case Reports, 2018 Crystal-storing histiocytosis (CSH) is a rare phenomenon in which crystalline material accumulates in the cytoplasm of histiocytes. Localized gastric CSH is an extremely rare condition.
Yasuko Fujita +7 more
doaj +1 more source
Leukemia cutis as the first manifestation of acute myeloid leukemia
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Florian Winkler +5 more
wiley +1 more source