HISTIOCITOMA FIBROSO MALIGNO PDF

Resumen. COLLAZO ALVAREZ, Hiralio; TORRECILLA SILVERIO, Dewar; MORALES FLORAT, Jorge Luis y COLLAZO MARIN, Stephens Yecc. Malignant. CASO CLÍNICO. Malignant oropharyngeal fibrous histiocytoma. Resection and radial reconstruction with fasciocutaneous flap. Histiocitoma fibroso maligno de. LETTERS TO THE EDITOR. Malignant fibrous histiocytoma – a rare hepatic tumor . Histiocitoma fibroso maligno, un tumor hepático raro.

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Histiocitoma fibroso maligno

Frequent mitotic figures were identified, some of them atypical. In 7 cases there was direct invasion of the adjacent organs and in two cases distant metastasis in the lungs and brain. In case of tumors in which adequate margins are not possible due to their location or large size, postoperative irradiation may improve control of the disease. This seems fibrlso be directly related with the extension of the resection 3,30 and presence or absence of residual disease.

Malignant fibrous histiocytoma of the head and neck: No fever, jaundice or pain. Head and neck sarcoma: Full text is only aviable in PDF.

Resection and radial reconstruction with fasciocutaneous flap. SNIP measures contextual citation impact by wighting citations based on the total number of citations in histlocitoma subject field.

Specialised Social Services Eurordis directory. They dibroso arrayed forming imbricated bundles and adopting a storiform growth pattern in areas, which confirmed the initial diagnosis.

Fibrosi Due to the sophisticated techniques necessary to diagnose this entity, and because of its differentiation with other types of sarcoma, we think that it is probably a neoplastic pathology much more frequently encountered than we realize. Patient died 45 days after admission. Malignant fibrohistiocytoma of the head and neck is an aggressive tumor.

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A 67 year old woman with several years history of clinically non-specific menometrorrhagias and occasional abdominal discomfort. No remarkable abnormalities in laboratory findings.

A propos of 3 cases of cervicofacial localization.

Orphanet: Histiocitoma fibroso maligno

In the skin, UPS presents as a relatively painless, rapidly enlarging nodule. This study supports the results obtained by other authors for MFH in other sites, such as Shinozaki et al. No cervical lymph nodes were palpated. The pleomophic-storiform type is the most common and is characterized as containing groups of spindle-shape neoplastic cells in a storiform pattern around blood vessels, in addition to histiocyte-like round cells that frequently exhibit a certain degree of pleomorphism Fig.

Cytologic features of a primary myxoid malignant fibrous histiocytoma arising in the uterus.

A meta-analysis published by the SMAC Sarcoma Meta- Analysis Collaboration on the individual data of patients treated with doxorubicin-based chemotherapy schedules is noteworthy regarding this point. Hepatic firoso fibrous histicytoma.

Ochandiano Caicoya 2J. Primary osseous UPS most commonly occurs in distal femur, proximal tibia, proximal femur and humerus.

In the myxoid variant, mesenchymal fiboso are present in a myxoid stroma rich in mucopolysaccharides. Malignant fibrous histiocytoma of the liver – a case report and review of the literature.

Acta Otorhinolaryngol Belg ; A retrospective study of cases. Abdomen was soft hitsiocitoma volumous with positive ascitic wave, tenderness in the right hypocondrium but no distinct hepatomegaly was found. It usually occurs in the deep planes of proximal extremities, in the retroperitoneum and in the trunk, although it can occur almost anywhere owing to its mesenchymal origin, including bone 1.

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J Laryngol Otol ; The rest of the physical examination and thoracoabdominal CAT found no tumoral spread. Haberal I, Samim E. Giant malignant fibrous histiocytoma of the uterus. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. UPS ranks the 4th most common soft tissue sarcoma with a slight male preponderance.

Undifferentiated pleomorphic sarcoma UPS is an aggressive sarcoma of soft tissues or bone that can arise from any part of the body, clinically presenting as swelling, mass, pain, pathological fracture and occasional systemic features and is characterized by high local recurrence and significant metastasis. However, other authors like Kearney et al.

A multicenter study of patients with multivariate analysis. A peak incidence is observed in the seventh decade and it is more frequent in men than in women.

With respect to the prognosis of MFH of the head and neck versus the limbs and trunk, the study of Sabesan et al. Health care resources for this disease Expert centres Diagnostic tests 4 Patient organisations 32 Orphan drug s