Intraparenchymal Brain Malignant Fibrous Histiocytoma
نویسندگان
چکیده
A 60-year-old man, with a history of hypercholesterolemia and left leg deep vein thrombosis, was admitted to hospital following two weeks of headaches and expressive aphasia. Neurological examination confirmed expressive aphasia in the absence of motor, sensory or cranial nerve deficit. A total body computer tomography (CT) imaging showed a single intraparenchymal lesion with a central necrotic area and peripheral edema in the left temporal lobe. MRI confirmed a single enhancing lesion of 25 mm on the left temporal lobe associated with perilesional edema (Figure 1). Positron emission tomography confirmed that there was no extra-cranial active disease. A radical left temporal craniotomy was performed and histopathological examination revealed an intraparenchymal mesenchymal tumor compatible with malignant fibrous histiocytoma (MFH). The pathologist described two different histological patterns: spindle cells forming fascicles and large neoplastic cell with foci of necrosis (Ki67 proliferation index: 70%). Post-operative course was complicated by fever. CT scan detected an infection in the surgical cavity, most likely Staphylococcus aureus. Consequently, intravenous antibiotic was administered for 6 weeks. A restaging MRI demonstrated a local recurrence associated with post-infection changes in the left temporal lobe (Figure 2). Despite a greater elapsed time following surgery than is usual (three months compared with an average of one month), adjuvant radiation treatment using 60 Gy in 30 fractions was administered. The patient died 18 months later from focal progressive disease.
منابع مشابه
Rothmund-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...
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 کاملMalignant Fibrous Histiocytoma in a Pigeon
Case Description- A pigeon with an abnormal mass on right wing was referred to the Veterinary Clinic of Shahid Bahonar University of Kerman. Treatment and Outcome- The mass was removed surgically and histopathologic examination was done. Microscopic findings revealed a stori-form pattern of atypical and pleomorphic spindle-shape tumor cells with histiocytes and too many thick wall capillari...
متن کاملMalignant Fibrous Histiocytoma در ماگزیلا: گزارش یک مورد و بررسی مقالات
سابقه و هدف: (MFH) Malignant Fibrous Histiocytoma، شایعترین سارکوم بافت نرم در بالغین بوده، اغلب در سنین بالا مشاهده می شود. این ضایعه بندرت در استخوان یافت می شود و در این صورت غالبا استخوان های دراز را مبتلا می کند و ابتلا استخوان های صورت و جمجمه به این ضایعه بسیار نادر است. به علاوه ماگزیلا، نسبت به سایر نواحی فک و صورت، محل شایعی برای بروز این ضایعه نیست. هدف از ارایه این مقاله، گزارش یک م...
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 کامل