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Cutaneous Inflammatory Malignant Fibrous Histiocytoma Presenting with a Leukemoid Reaction: A Case Report and Review of the Literature

机译:皮肤炎症性恶性纤维组织细胞瘤伴类白血病反应:一例报道并文献复习

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Malignant fibrous histiocytoma (MFH) is the most common sarcoma found in adults. We discuss a case of inflammatory MFH of dermal/epidermal origin presenting with a severe leukemoid reaction (LR). A 60 years old white male presented to hematology/oncology clinic complaining of mild shortness of breath on exertion. Past medical history was remarkable for removal of a left upper extremity necrotic mass 4.4 × 3 × 3 cm. Microscopy of the specimen showed clear surgical margin, and tumor cells restricted to the dermis without lymphovascular invasion. Immunohistochemestry was positive for CD 68 and CD 99. Chest x-ray was negative for metastatic disease. White blood cell count was 109.4 k/mm3with 24 k/mm3band neutrophils, and absolute neutrophil count of 69 k/mm3. CT scan of the thorax revealed numerous bilateral pulmonary nodules suspicious for metastasis. Based on these findings patient was diagnosed with metastatic cutaneous IMFH associated with a LR. Following review of medical literature, this appears to be the first reported case of inflammatory cutaneous MFH associated with LR. This histological variant is rare, and carries a poor prognosis. Thus, we would like to emphasize the need for investigating alternative therapies capable of improving the survival of these patients.
机译:恶性纤维组织细胞瘤(MFH)是成年人中最常见的肉瘤。我们讨论皮肤/表皮起源的炎症性MFH伴有严重的类白血病反应(LR)。一名60岁的白人男性到血液学/肿瘤科门诊,抱怨劳累时轻度呼吸急促。过去的病史对于去除左上肢坏死性肿块4.4×3×3 cm而言非常显着。标本的显微镜检查显示清晰的手术切缘,肿瘤细胞局限于真皮,无淋巴管浸润。免疫组织化学法对CD 68和CD 99呈阳性。胸部X射线对转移性疾病呈阴性。白细胞计数为109.4 k / mm3,带中性粒细胞为24bandk / mm3,绝对中性粒细胞计数为69 k / mm3。胸部的CT扫描显示大量双侧肺结节可疑转移。基于这些发现,患者被诊断出与LR相关的转移性皮肤IMFH。根据医学文献的审查,这似乎是首次报道的与LR有关的炎症性皮肤MFH病例。这种组织学变异很少见,预后差。因此,我们想强调需要研究能够改善这些患者生存率的替代疗法。

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