Results 1 to 10 of about 31,396 (267)
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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Xanthogranulomatous Cholecystitis: CT and USG Characteristics [PDF]
Cholecystitis is a common finding in everyday practice of ultrasound. The diagnosis of Xanthogranulomatous Cholecystitis (XGC) is however an uncommon entity and every radiologist should be aware of the characteristic ultrasound and CT findings to ...
Siddarth Ragupathi, Sahadevan Vijay
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Cetacean morbillivirus (CeMV; Paramyxoviridae) causes epizootic and interepizootic fatalities in odontocetes and mysticetes worldwide. Studies suggest there is different species-specific susceptibility to CeMV infection, with striped dolphins (Stenella ...
Josué Díaz-Delgado +24 more
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Malakoplakia of Bone Presenting as Bilateral Septic Arthritis: A Case Report [PDF]
Malakoplakia is an uncommon chronic inflammatory disorder that usually involves an abnormal immunological response to underlying infection. Though it is reported in almost every organ system, involvement of bone is extremely rare, where it usually ...
S Supriya, B Krishnamoorthi Adiga
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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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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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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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Non-Langerhans-Cell histiocytosis spectrum of disorders includes multicentric reticulohistiocytosis (MR) and multiple cutaneous reticulohistiocytomas (MCR), which are very uncommon granulomatous conditions. In reticulohistiocytoma, the most common sites
Karuna Singh Sijapati +2 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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Langerhans cell histiocytosis: unusual bone marrow infiltration—report of 2 cases in Ecuador
Langerhans cell histiocytosis (LCH) is a histiocytic neoplasm characterized by the abnormal proliferation of Langerhans cells. Bone marrow (BM) involvement is associated with high-risk disease and poor survival.
Paulina Santana +3 more
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