• 대한골관절종양학회지
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• 제1권1호
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• pp.77-83
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• 1995

1. 연부 조직과 골 조직사이에서의 악성 섬유성 조직구종의 근본적인 조직학적 차이는 없었다. 2. 악성 섬유성 조직구종은 조직학적 소견이 다양하므로, 확진을 위해서는 다른 종양을 반드시 배제하여야한다. 3. 재발시 다른 형태의 조직 소견을 보여줄 수 있기 때문에 정확한 진단을 위해 환자의 과거력 및 과 거의 조직학적 검토가 필수적이라 사료된다.

• Journal of Chest Surgery
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• 제33권9호
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• pp.770-772
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• 2000

Primary malignant fibrous histocytoma(MFH) of pleura is very rare. Upon microscopic examination, the tumor was characterized by storiform pattern of growth and intense, diffuse immunostaining for $\alpha$ l-antichymotripsin. We report a case of primary malignant pleural fibers histiocytoma with extension to lung, which was managed by complete excision of pleural mass and lobectomy with thoracoplasty.

• 대한후두음성언어의학회지
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• 제22권2호
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• pp.159-161
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• 2011

Malignant fibrous histiocytoma is one of the rare types of larynx tumor. The most common sites of the tumor are limbs, trunk, and retroperitoneal space, but tumor localization within head and neck are very rare. It is built of histiocytes, fibroblasts and multinuclear giant cells. A diagnosis of the tumor includes microscopic and immunohistologic examination with identification of specific tissue markers and intermediate filaments of proteins. This disease has been treated by several methods combining radical surgery, radiotherapy, and chemotherapy, but the prognosis is poor. We present 74-year-old Asian man with dysphonia for 2 years. The tumor of the larynx was examined on laryngoscopy. The radical surgery rendered the final pathological diagnosis, confirmed histologically and immunohistochemically as malignant fibrous histiocytoma. This tumor was treated with laser cordectomy followed by radiotherapy. 3.5 year's observation of the patient didn't either show any signs of recurrence or dysphonia.

• 대한두경부종양학회지
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• 제17권2호
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• pp.230-233
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• 2001

Malignant fibrous histiocytoma (MFH) is a sarcoma that occurs principally in soft tissue and typically involved the skeletal muscle and deep fascia. Although it is one of the most common types of soft tissue sarcoma in late adult life, the involvement of the head and neck area is relatively rare. MFH shows variable histologic appearance, and may be classified into several subtypes(storiform-pleomorphic, myxoid, giant cell, inflammatory, angiomatoid) and the storiform-pleomorphic type is the most common type. The authors have recently experienced a case of MFH in the right maxillary sinus, and report it with a brief review of the related literature.

• Journal of Chest Surgery
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• 제24권4호
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• pp.357-360
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• 1991

Malignant fibrous histiocytoma is the most common soft tissue sarcoma of late adult life. The tumor occurs principally in one of the extremities or in the abdominal cavity or retroperitoneum, but very rarely in the heart. We report a case of M.F.H. that arose from the posterior wall of the left atrium. A 50 years old woman was presented with signs and symptoms of severe congestive heart failure. On 2-D echocardiographic exam, a huge mass was found in the left atrium. The mass was excised under open heart surgery. Histologic examination revealed that the tumor was actually a malignant fibrous histiocytoma.

• 대한기관식도과학회지
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• 제7권1호
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• pp.46-49
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• 2001

Fibrous histiocytoma is the soft tissue tumor of histiocytic origin that have a variety of histological patterns. Although cases of malignant fibrous histiocytoma in the head and neck have been reported increasing frequency in recent years, they are rare conditions. We reporeted a case of malignant fibrous histiocytoma of the trachea in which the Patient had been given laryngomicrosurgical biopsy for subglottic mass. Prognosis of malignant fibrous histiocytoma, the use of radiation as primary treatment, and its role in the development of secondary primary tumors in the head and neck region are reviewed.

• Tuberculosis and Respiratory Diseases
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• 제54권6호
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• pp.645-650
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• 2003

저자들은 우측 흉부 불편감을 주소로 내원한 25세 여자 환자를 개흉 조직 검사를 시행하여 원발성 횡격막 기원 악성 섬유성 조직구종을 진단하였고 ifosfamide, doxorubicin으로 항암 화학 요법 시행 후 부분 관해가 있었으나 진단 후 12개월째 외래 추적 검사 중 뇌전이로 사망한 젊은 여성 1예를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

• 대한골관절종양학회지
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• 제14권2호
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• pp.119-124
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• 2008

서론: 악성 연부 조직의 광범위 절제술 후 발생한 연부 조직 결손에 대해 전외측 대퇴부 유리 피판 이식술로 재건술을 시행한 7예에 대해서 치료 결과 및 그 유용성에 대해 알아 보고자 한다. 대상 및 방법: 2003년 1월부터 2007년 6월까지 연부조직 악성 종양으로 광범위 절제술 후 전외측 대퇴부 유리 피판을 이용한 재건술을 시행 받은 7예를 대상으로 하였다. 연구 방법은 임상 기록의 검토를 통해 후향적으로 시행하였으며, 종양의 종류, 크기, 종양의 절제연, 종양 절제 후 연부 조직 결손의 크기, 피판의 성공여부, 수술 시간, 합병증 등을 조사하였다. 결과: 악성 연부 조직 종양은 활막 육종이 3예, 악성 섬유성 조직구종이 2예, 평활근 육종이 1예, 섬유육종이 1예였다. 종양의 크기는 $3{\times}5\;cm$부터 $7{\times}8\;cm$로 다양하였고, 모든 예에서 광범위 절제연을 얻을 수 있었다. 종양 절제 후 피부 연부 조직 결손의 크기는 $6{\times}8\;cm$부터 $15{\times}10\;cm$였고, 평균 수술 시간은 3.6시간이었다. 모든 예에서 이식된 피판은 생존하였다. 결론: 악성 연부 조직의 수술적 치료에 있어 전외측 대퇴부 유리 피판술은 종양의 광범위한 절제술 후에도 적절한 크기와 길이의 혈관경을 확보할 수 있으며, 공여부의 합병증을 최소화하며, 미용적으로 우수하여 종양 절제 후 연부조직의 재건에 유용한 술식으로 사료된다.

• Journal of Chest Surgery
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• 제20권2호
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• pp.358-366
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• 1987

A case of malignant fibrous histiocytoma [MFH] of left pulmonary artery was reported in the 27 year-old male. He was admitted because of hemoptysis for several times. Chest x-ray revealed nodular lesions in left hilar area and left upper lobe. A left thoracotomy was performed followed left upper lobectomy. The main tumor was originated from the pulmonary arterial bifurcation and proximal portion of the left pulmonary artery. By light microscopy, there were many pleomorphic giant cells, which displayed the storiform pattern. And in those area, dilated or compressed vascular channels were involved by tumor cells, suggesting origin of This tumor. Pulmonary artery angiography and chest CT revealed this tumor was originated from pulmonary artery. It would be the first reported primary malignant fibrous histiocytoma of the pulmonary artery in our country. Postoperative prognosis was uneventful, but recently he was suffered from dyspnea, that was noticed by OVD follow-up for 1 month, probably the heart failure sign due to pulmonary arterial flow obstruction.

• 대한세포병리학회지
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• 제6권1호
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• pp.80-83
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• 1995

Malignant fibrous histiocytoma is the most common soft tissue sarcoma of late adult life, but it is rare in the pleura. We recently experienced a case of cytology of malignant fibrous histiocytoma in plural fluid. The smear revealed histiocytic malignant cells, spindle malignant cells and inflammatory cells. The histiocytic cells showed abundant, pale cytoplasm and ovoid, irregular eccentrically-placed nuclei. The spindle cells showed elongated nuclei. Intercellular collagen was also present.