伪装成慢性血肿的软组织肉瘤1例报告及文献复习。

Amit Gupta, Aditya Menon, Manish Agarwal, Vikas M Agashe
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引用次数: 0

摘要

简介:在罕见的情况下,软组织肉瘤可能类似于肌肉内血肿。我们提出一个病例的病人诊断为多形性梭形细胞肉瘤,出现类似于肌肉内血肿。病例报告:一名45岁男性表现为左大腿疼痛、肿胀和脓区。成像显示软组织中有气体,患者表现出严重疾病的迹象,包括血液检查异常。在深入研究他的病史后,发现他经历了一次轻微的跌倒,之后他的大腿在6个月的时间里逐渐肿胀。最初,磁共振成像(MRI)诊断为血肿。外科医生在没有进行培养或组织病理学检查的情况下进行了探查性手术和引流。两周后,该部位受到感染,根据放射检查结果显示是感染的血肿,需要进行第二次手术。深层组织培养培养出鲍曼不动杆菌。大腿x线片显示软组织内有空气。病人因怀疑气性坏疽被转介到我院。在提出的时候,MRI显示一个不均匀的肿块,导致咨询骨科肿瘤学家。术中冰冻切片分析显示为梭形细胞肿瘤。骨科肿瘤外科小组进行了大规模切除,随后使用真空辅助闭合进行了额外的清创。从深层组织培养中分离出阴沟肠杆菌,这可能解释了软组织中观察到的气囊的存在。随后,进行大面积切除肉瘤,用皮肤移植覆盖伤口。7个月后,患者因肺转移而接受化疗,手术部位无感染迹象。患者在本院首次就诊12个月后因肿瘤转移死亡。结论:医疗保健专业人员在处理创伤后肌肉内血肿时应高度谨慎。虽然MRI结果可以帮助诊断,但将其与临床表现结合起来考虑是至关重要的。为了最终排除癌症的可能性,活检和组织病理学分析是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Soft Tissue Sarcoma Masquerading as Chronic Hematoma: A Case Report and Literature Review.

Introduction: Soft tissue sarcomas may resemble intramuscular hematomas in rare instances. We present a case of a patient diagnosed with pleomorphic spindle cell sarcoma that appeared similar to an intramuscular hematoma.

Case report: A 45-year-old male presented with a painful, swollen, and pus-discharging area on his left thigh. Imaging revealed gas in the soft tissues, and the patient exhibited signs of severe illness, including abnormal blood work. Upon delving into his medical history, it was revealed that he had experienced a minor fall, after which his thigh gradually swelled over 6 months. Initially, an magnetic resonance imaging (MRI) diagnosed the condition as a hematoma. A surgeon performed an exploratory procedure and drainage without obtaining cultures or conducting a histopathological exam. Two weeks later, the site became infected, necessitating a second surgery based on radiological findings suggesting an infected hematoma. Deep tissue cultures grew Acinetobacter baumannii. Radiographs of the thigh showed air in soft tissues. The patient was referred to our institute suspecting gas gangrene. At the time of presentation, MRI showed a heterogeneous mass, leading to consultation with an orthopedic oncologist. Intraoperative frozen section analysis indicated a spindle cell neoplasm. The orthopedic oncosurgery team proceeded with en-masse excision, followed by additional debridement using vacuum-assisted closure. Enterobacter cloacae was isolated from deep tissue cultures, likely explaining the presence of gas pockets observed in soft tissues. Subsequently, a wide excision of the sarcoma was carried out, with skin grafting to cover the wound. Seven months later, the patient was undergoing chemotherapy for pulmonary metastases, with the surgical site showing no signs of infection. The patient succumbed to the disease 12 months after initial presentation at our institution, with metastasis being the cause of death.

Conclusion: Healthcare professionals should exercise heightened caution when managing post-traumatic intramuscular hematomas. Although MRI results can aid in diagnosis, it is vital to consider them alongside clinical findings. To conclusively exclude the possibility of cancer, a biopsy followed by histopathological analysis is necessary.

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