Kim Jong Gwang, Sung Woo Jin, Kim Dong Hwan, Kim Young Hwan, Sohn Sang Kyun, Lee Kyu Bo
Department of Oncology/Hematology, Kyungpook National University Hospital, Daegu, Korea.
Korean J Intern Med. 2005 Mar;20(1):100-4. doi: 10.3904/kjim.2005.20.1.100.
A malignant peripheral nerve sheath tumor (MPNST) is an extremely rare soft tissue tumor in the general population. On the other hand, there is a higher incidence of MPNST in patients with neurofibromatosis type I (von Recklinghausen's disease). The common sites are the extremities, trunk, head and neck. However, an intraabdominal or intrathoracic manifestation is uncommon. This paper reports two patients, a 31 year-old woman with multiple neurofibromatosis presenting as an intraabdominal malignant peripheral nerve sheath tumor, and a 33 year-old woman with an intrathoracic malignant peripheral nerve sheath tumor. The patients were treated with chemotherapy followed by radiotherapy. However, one patient died as a result of disease progression 21 months after the diagnosis and the other patient is currently being treated with radiotherapy.
恶性外周神经鞘瘤(MPNST)在普通人群中是一种极其罕见的软组织肿瘤。另一方面,I型神经纤维瘤病(冯·雷克林豪森病)患者中MPNST的发病率较高。常见部位为四肢、躯干、头颈部。然而,腹内或胸内表现并不常见。本文报告了两名患者,一名31岁患有多发性神经纤维瘤病的女性,表现为腹内恶性外周神经鞘瘤,另一名33岁女性患有胸内恶性外周神经鞘瘤。患者接受了化疗,随后进行放疗。然而,一名患者在诊断后21个月因疾病进展死亡,另一名患者目前正在接受放疗。