Pulmonary sarcoma complicated with neurofibromatosis type 1 (NF1)

被引:0
|
作者
Abe, Y
Hatanaka, H
Kamiya, T
Yamazaki, H
Kijima, H
Inoue, H
Ueyama, Y
Nakamura, M [1 ]
机构
[1] Univ Tokyo, Sch Med, Dept Pathol, Kanagawa 2591193, Japan
[2] Univ Tokyo, Sch Med, Dept Surg, Kanagawa 2591193, Japan
[3] Natl Kanagawa Hosp, Dept Resp Dis, Kanagawa 2578585, Japan
关键词
pulmonary sarcoma; neurofibromatosis type 1 (NF1); empyema; actinomycosis; von Recklinghausen's disease;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We report here a case of primary pulmonary sarcoma complicated with neurofibromatosis type 1 (NF1). A 60-year-old man was urgent admitted to Tokai University Hospital, Japan, due to severe right chest pain. Skin inspection showed subcutaneous tumor lesions and cafe-au-lait spots, and therefore a diagnosis of neurofibromatosis type 1 (NF1) was made. Chest X-ray showed marked fluid accumulation in the right pleural cavity, and he was diagnosed as having empyema by thoracic drainage. Chest X-ray showed a large round mass lesion (80 mm in diameter) in the right lower lung field. Percutaneous needle biopsy of the tumor revealed that the empyema was caused by actinomycotic infection, and then he underwent right middle and lower lobectomy. Histopathological examination of the surgical specimens revealed features of spindle cell sarcoma. Several postoperative systemic examinations showed no other lesions except in the right lung. We concluded that this was a complicated case of primary pulmonary sarcoma with NF1.
引用
收藏
页码:613 / 616
页数:4
相关论文
共 50 条
  • [1] Seizures in neurofibromatosis - Type 1 (NF1)
    Kulkantrakorn, K
    Geller, TJ
    NEUROLOGY, 1997, 48 (03) : 6007 - 6007
  • [2] The role of NF1 pseudogenes in the development of neurofibromatosis type 1 (NF1)
    Luijten, M
    Bijleveld, EH
    Westerveld, A
    Hulsebos, TJM
    EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 : 146 - 146
  • [3] Osteoporosis in neurofibromatosis type 1 (NF1).
    Poyhonen, M
    Heikkinen, J
    Väänänen, K
    Peltonen, J
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 124 - 124
  • [4] A novel neurofibromatosis type 1 (NF1) mutation in a patient with NF1 and pheochromocytoma
    Seo, Yoorim
    Jeong, Yeonjeong
    Kim, Dong Yoon
    Choi, Kyueun
    Kim, Eun Sook
    Moon, Sung Dae
    Han, Je Ho
    KOREAN JOURNAL OF INTERNAL MEDICINE, 2018, 33 (01): : 214 - 217
  • [5] Cardiovascular malformations in neurofibromatosis type 1 (NF1).
    Friedman, JM
    Birch, PH
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A98 - A98
  • [6] Mutation screening in neurofibromatosis type 1 (NF1)
    Park, VM
    Sturtevant, DB
    Kenwright, KA
    Pivnick, EK
    AMERICAN JOURNAL OF PATHOLOGY, 1998, 153 (05): : 1652 - 1652
  • [7] Neurofibromatosis type 1 (NF1) and Associated Tumors
    Rosenbaum, T.
    Wimmer, K.
    KLINISCHE PADIATRIE, 2014, 226 (6-7): : 309 - 315
  • [8] Molecular genetics of neurofibromatosis type 1 (NF1)
    Shen, MH
    Harper, PS
    Upadhyaya, M
    JOURNAL OF MEDICAL GENETICS, 1996, 33 (01) : 2 - 17
  • [9] Choroidal Findings in Neurofibromatosis Type 1 (NF1)
    Giannini, Caterina
    Rodriguez, Fausto
    Eberhart, Charles
    Salomao, Diva
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2010, 69 (05): : 548 - 548
  • [10] Lymphomas in patients with neurofibromatosis type 1 (NF1): another malignancy in the NF1 syndrome?
    Fareez, Faiha
    Wang, Bill H.
    Brain, Ian
    Lu, Jian-Qiang
    PATHOLOGY, 2023, 55 (03) : 302 - 314