A case of malignant fibrous histocytoma reconstructed using cervico-facial flap.
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چکیده
منابع مشابه
Malignant fibrous histocytoma producing spinal cord compression.
Three cases of malignant fibrous histiocytoma presented as primary paraspinal tumours causing extradural spinal cord compression. Study of these cases suggests that pain relief is considerable after laminectomy but pain may recur with further tumour growth. Total removal is unrealistic and diagnosis, difficult. The prognosis in terms of continuing neurological deficit after surgery followed by ...
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SUMMARY Occurance of Malignant Fihrous Histiocytoma (MFH) of the spermatic cord as a primary source is so rare that since I 967 Just 12 of such cases have heen reported (4,8, 10). MFH is one of the pleomorphic soft tissue Malignant tumors which has been studied for first time by Ozzello and Co workers on 1963. The Tumor ong1nates from primary Mesenchymal cells which have both histocytic & fi...
متن کاملMalignant Fibrous Histiocytoma of the Lung: A Case Report
Malignant Fibrous Histiocytoma (MFH) is the most common soft-tissue sarcoma which predominantly surfaces in the retro-peritoneum and extremity. MFH of lung is a very rare condition. The diagnosis is essentially through histologic examination. However, the invasion of the chest wall or other organs might help establish the malignant nature.We report a case of a 77-year-old man who had been prese...
متن کاملMetachronous Malignant Fibrous Histiocytoma- A Rare Case Report
Malignant fibrous histiocytoma (MFH) is one of the most common types of soft tissue sarcomas in adults. Distant metastases are developed in 30–40% of patients with MFH, with the most common site being the lung. However, metachronous MFH has not been reported previously in literature. This report describes a case of a 30-year-old man, who had two metachronous thigh tumors, both of which were con...
متن کاملRothmund-Thomson Syndrome with Malignant Fibrous Histiocytoma: Report of a Case and Review of Literature
Rothmund–Thomson syndrome is a rare autosomal recessive genodermatosis characterized by early onset of poikiloderma and several other cutaneous and organ involvements. We are going to report a 14-year-old girl who has been diagnosed with Rothmund– Thomson syndrome since she was 3 years old and has been suffering from pain and swelling of the right elbow and forearm for about 6 months. There are...
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ژورنال
عنوان ژورنال: Skin Cancer
سال: 1999
ISSN: 1884-3549,0915-3535
DOI: 10.5227/skincancer.14.52