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histiocytic sarcoma/muntah
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Malignant histiocytosis with central nervous system involvement and hepatic mucinous cystadenoma in a single patient with review of the literature.
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Malignant histiocytosis is a rare neoplasm of the reticuloendothelial system characterized by neoplastic proliferation of tissue histiocytes. We report a case of malignant histiocytosis in a 64-year-old female initially operated on for a mucinous cystadenoma of her liver. Four months after the
Primary histiocytic sarcoma of the brain mimicking cerebral abscess.
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Histiocytic sarcoma is a rare malignancy with only 10 reports confirmed primarily involving the CNS. The diagnosis is dependent on the finding of malignant cells with histiocytic morphology and immunophenotype. The authors report a case of pathologically proven HS of the CNS. A 16-year-old boy
Primary cerebral histiocytic sarcoma in childhood: a case report of protracted survival and review of the literature.
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BACKGROUND
Histiocytic sarcoma (HS) of the central nervous system (CNS) is exceptionally rare in pediatric patients, historically associated with an exceptionally poor prognosis. Here, the authors present a novel case of protracted progression-free survival following surgical excision, radiotherapy
Pediatric intracerebral histiocytic sarcoma with rhabdoid features: Case report and literature review.
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A 16-year-old boy presented with marked weight loss, weakness of the left extremities and dizziness of 2 months duration and vomiting for 2 days. Brain MRI showed an approximately 6.5 × 5.3 cm-sized huge heterogeneous enhancing mass located in the corpus callosum, extending into the lateral
Primary histiocytic sarcoma of the central nervous system: a case report with platelet derived growth factor receptor mutation and PD-L1/PD-L2 expression and literature review.
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BACKGROUND
Histiocytic sarcoma (HS) is an aggressive malignant neoplasm. HS in the central nervous system is exceptionally rare and associated with a poor prognosis. This report documents a case of primary HS of the central nervous system with treatment including surgery, radiotherapy, and
[A localised histocytic sarcoma in the stomach of a dog].
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A 6-year-old neutered female Bernese mountain dog is described with anorexia, weight loss and melena. Gastric neoplasia was noticed (on ultrasound) and pathological examination ofgastric biopsies showed a histiocytic tumor. Necropsy confirmed the diagnosis of a localised histiocytic sarcoma. It was
[Mucinous cystadenomas of the liver].
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BACKGROUND
Biliary cystadenomas of the liver are rare benign tumors prone to malignant alteration so that a total excision is recommended.
OBJECTIVE
The aim of the paper is to present our experience in treatment and to evaluate whether a simple ablation represents the appropriate
Gamna-Gandy bodies: a case of mistaken identity in the spleen of a cat.
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A 4-year-old, female spayed Domestic Shorthair cat was presented for a 2-day history of lethargy, anorexia, and vomiting. Diagnostic assessments revealed a severe, regenerative anemia and the presence of a solitary, 3 × 4 cm splenic mass. Cytologic examination of fine-needle aspirates of the splenic
Unusual histiocytic disease in a Somali cat.
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An 8-year-old Somali cat presented with a 9-month history of inappetence, vomiting and weight loss. The disease progressed to involve neurological signs associated with a mass lesion at the level of the first lumbar vertebra. Histopathology identified the condition as malignant histiocytosis
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