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desmos chinensis/kanker
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8 hasil
Eruptive dermal clear cell desmo-plastic mesenchymal tumors with perivascular myoid differentiation in a young boy. A clinical, histopathologic, immunohistochemical and electron microscopy study of 17 lesions.
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Clear cell tumors of the skin are observed in a wide variety of benign and malignant conditions with different histogenesis, sharing the presence of cells with abundant clear cytoplasm. Herein, we report the clinicopathologic features of a healthy young patient affected by asymptomatic, eruptive and
[Psammous desmo-osteoblastoma of the right maxilla. Case report and differential diagnosis of a rare tumor].
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METHODS
We report the case of a 9-year-old female patient with a moderate swelling of the right maxilla. A tumor was diagnosed by conventional X-ray within the region of tooth 17 in the right tuber maxillae. The histological diagnosis after biopsy of the lesion was "fibrous dysplasia
[New conceptual aspects in the diagnosis of fibro-osseous lesions of the maxillofacial skeleton. IV. Osteoblastic tumors occurring in the dentigerous and other skull bones (trabecular and psammous desmo-osteoblastomas].
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[Studies on chemical constituents in the root of Desmos grandifolius (I)].
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OBJECTIVE
To investigate new compounds with anti-tumor activities from the root of Desmos grandifolius of Annonaceae.
METHODS
The chemical constituents were isolated by silica gel column chromatography, and the structures were elucidated by UV, IR, MS, 1H NMR, 13C NMR, H-H COSY and NOESY
Design, synthesis, and antitumor activity of desmosdumotin C analogues.
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Desmosdumotin C (Des C), a natural product isolated from the roots of Desmos dumosus, has shown good antitumor activity. A three dimensional quantitative structure-activity relationship (QSAR) study using the comparative molecular field analysis (CoMFA) method was performed on 32 Des C
Psammous desmo-osteoblastoma. Ultrastructural and immunohistochemical evidence for an osteogenic histogenesis.
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Fibro-osteo-cemental lesions of the jaw bones are a heterogeneous group of diseases which present problems in classification. Psammous desmo-osteoblastoma is one of four newly proposed entities (Makek 1983) and has until now been characterized by its light microscopic, clinical and radiological
The desmo- and osteoplastic ameloblastoma. Histologic variant or clinicopathologic entity? Case reports.
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Two cases of desmoplastic ameloblastoma (DA) are presented, bringing the total number of reported cases to 29. One case of the so-called "hybrid lesion" is added to the presentation. Immunohistochemical studies indicate that the desmoplasia is caused by active de novo synthesis of extracellular
Psammous desmo-osteoblastoma with concomitant aneurysmal bone cyst of mandible.
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Juvenile psammomatoid ossifying fibroma is a gradually progressive, aggressive extragnathic craniofacial tumor of bone. Due to its complex histogenesis, biological behavior, histology, and classification, its nomenclature has always been the focus of debate among pathologists. Based on the clinical
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