Results 11 to 20 of about 840 (50)
Background: Oral exfoliative cytology includes the study and interpretation of the features cells exfoliated from the oral mucosa. The aim of this study was to analyze cytological changes in the periodontal pocket of patients with different clinical ...
E Castro Cecilia+2 more
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Xanthogranulomatous Inflammation of Colon: A Case Report [PDF]
Xanthogranulomatous Inflammation (XGI) is a rare pathological condition that can affect various organs, such as lungs, endometrium, vagina, fallopian tube, ovary, testis, stomach, colon, appendix and pancreas.
Ramya Lakshminarayanan+3 more
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Atualmente, os histiócitos não são mais compreendidos como células únicas, mas como um grupo heterogêneo de células com o mesmo aspecto histológico, mas com características e funções distintas entre si.
Flávio Barbosa Luz+3 more
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Benign fibrohistiocytic tumour of the palate
Benign fibrous histiocytomas of soft tissue are composed of spindled fibroblasts admixed with secondary elements including histiocytes, foam cells, and inflammatory cells. These tumors occur equally in males and females and most often arise in the dermis
Nilima Sharma, Mohammad Jaseem Hassan
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Xanthogranulomatous Oophoritis: A Rare Case Report [PDF]
Background and Objective: Xanthogranulomatous oophritis is an uncommon, non-neoplastic, chronic process in which the affected organ is destroyed by massive cellular infiltration of foamy histiocytes admixed with multinucleated giant cells, plasma cells ...
Kaneeka Bhatnagar+3 more
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Indeterminate cell tumor (Histiocytosis)
Indeterminate cell tumor (ICT; histiocytosis) is a rare disorder characterized by accumulation of histiocytes that do not fulfill the phenotypic criteria designated for Langerhans cells (LC).
Ayesha Ahmed+6 more
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First described in 1930 as a lipoid granulomatosis, Erdheim-Chester disease (ECD) is a rare histiocytosis encompassing a group of disorders caused by overproduction of histiocytes, a subtype of white blood cells. This disease most commonly involves the
Hyuk Gi Hong+3 more
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Cerebral manifestation and diagnostic dilemma of Rosai-Dorfman disease
Rosai-Dorfman disease (RDD) is a rare, S100-positive histiocytic proliferation, that can cause both nodal and extranodal illness. We present a case of a 53-year-old male patient.
Szintia Almási+3 more
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Cutaneous and Nodal Histiocytic Sarcoma: A Series of Five Cases [PDF]
Histiocytic Sarcoma (HS) is an extremely rare haematolymphoid neoplasm that exhibits morphological and immunophenotypic features indicative of histiocytic differentiation.
Geeta Yadav+4 more
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Benign Fibrous Histiocytoma: An Uncommon Presentation [PDF]
Intracranial fibrous histiocytomas are rare; Benign Fibrous Histiocytoma (BFH) being uncommon than its malignant counterpart. BFH comprises fibroblasts and histiocytes without any nuclear pleomorphism or atypia.
SAGARIKA SARKAR+3 more
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