The Experts below are selected from a list of 39 Experts worldwide ranked by ideXlab platform

Liu Xin-mi - One of the best experts on this subject based on the ideXlab platform.

  • Clinical analysis of 25 patients with Malignant Neurilemoma
    Chinese clinical oncology, 2007
    Co-Authors: Liu Xin-mi
    Abstract:

    Objective:To analyse the clinical characteristics of Malignant neurilenoma to improve our knowledge of this disorder. Methods:Twenty-five patients were retrospectively reviewed with Malignant Neurilemoma admitted to our hospital from Jan 1993 to Feb 2006. Results:The patient group included 14 (56%) males and 11 (44%) females with a mean age of 53.7 years (range, 20-84 years). Sixteen(64%) cases presented with body surface masses, 7 (28%) cases with abdominal cavity or pelvic cavity masses, 1 case with backache and low limb weakness, 1 case found lung nodules on health examination. Histologically all the specimens were composed of spindle cells, 24 (96%) cases were immunohistochemically positive for S-100 protein, and 1 (4%) case negative. Twenty-three(92%) cases underwent tumor resection totally or partially, 1 case had no operation, 1 case underwent exploratory laparotomy to find extend metastasis impossible for resection. Six cases were given radiotherapy post operation, 2 cases given transcatheter arterial chemotherapy pre-operation. Twenty-five cases were followed-up from 7 months to 5 years, 4 (16%) cases had lung metastasis, 2 (8%) cases had lymphonode metastasis, 7 (28%) cases had recurrence, 10 (40%) cases had not been found metastasis or recurrence. Conclusion:Malignant Neurilemoma may occur all over the body, most often on body surface. Last diagnosis depends on pathologic examination. The tumor is apt to recurrence and metastasis, and surgery is the most effective therapy for it.

Li-na Wang - One of the best experts on this subject based on the ideXlab platform.

  • Malignant Neurilemoma with xeroderma pigmentosum
    Case Reports, 2009
    Co-Authors: Li-na Wang, Min Jian
    Abstract:

    Xeroderma pigmentosum is a rare autosomal recessive disease characterised by hypersensitivity to sunlight, and is associated with a high incidence of skin cancer. We report a case of xeroderma pigmentosum with Malignant Neurilemoma in a 46-year-old woman which is unique due to its presentation, which was confirmed histopathologically. Trial registration number: 31095

  • Malignant Neurilemoma with xeroderma pigmentosum
    BMJ Publishing Group, 1
    Co-Authors: Li-na Wang, Ma, Min Jian, Shi, Ji Tong
    Abstract:

    Xeroderma pigmentosum is a rare autosomal recessive disease characterised by hypersensitivity to sunlight, and is associated with a high incidence of skin cancer. We report a case of xeroderma pigmentosum with Malignant Neurilemoma in a 46-year-old woman which is unique due to its presentation, which was confirmed histopathologically

Min Jian - One of the best experts on this subject based on the ideXlab platform.

  • Malignant Neurilemoma with xeroderma pigmentosum
    Case Reports, 2009
    Co-Authors: Li-na Wang, Min Jian
    Abstract:

    Xeroderma pigmentosum is a rare autosomal recessive disease characterised by hypersensitivity to sunlight, and is associated with a high incidence of skin cancer. We report a case of xeroderma pigmentosum with Malignant Neurilemoma in a 46-year-old woman which is unique due to its presentation, which was confirmed histopathologically. Trial registration number: 31095

Shi, Ji Tong - One of the best experts on this subject based on the ideXlab platform.

Bao-fa Hong - One of the best experts on this subject based on the ideXlab platform.

  • Clinical analysis of 7 cases of adult prostate sarcoma
    Zhonghua nan ke xue = National journal of andrology, 2004
    Co-Authors: Zhen Wang, Jiang-ping Gao, Xiao-xiong Wang, Liquan Zhou, Bao-fa Hong
    Abstract:

    Objective To investigate the diagnosis, treatment and prognosis of adult prostatic sarcoma. Methods The records of 7 patients with prostate sarcoma were reviewed in the light of clinical manifestation, laboratory examination, therapeutic methods and histological subtypes. Several clinicopathological variables were assessed for prognostic significance. Results Of the 7 cases, 3 were leiomyosarcoma, 3 rhabdomyosarcoma and the other Malignant Neurilemoma. Most patients presented urinary obstruction, and the diagnosis of prostate sarcoma was established with ultrasound guided biopsy. Histological subtypes were related to the rate of survival. Two patients received radical cystoprostatectomy and died 13 and 21 months respectively after operation. Two cases underwent total pelvic exenteration, followed by chemotherapy and/or radiotherapy and still alive 15 months after operation. The other 3 received only chemotherapy and/or radiotherapy and died 7 months on average after diagnosis. Conclusion The long-term survival rate for adults with prostate sarcoma is low. Early diagnosis and complete surgical resection offer patients the best chance for survival. Long-term surveillance is necessary for the early detection of recurrence.