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首页> 外文期刊>International Journal of Surgery Case Reports >Cystic poorly differentiated squamous cell carcinoma of the scalp, a rare scalp tumor: Case report and literature review
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Cystic poorly differentiated squamous cell carcinoma of the scalp, a rare scalp tumor: Case report and literature review

机译:头皮囊性低分化鳞状细胞癌,一种罕见的头皮肿瘤:病例报告和文献复习

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Introduction Cutaneous cystic lesions have broad differentials ranging from common benign entity to rare malignant lesions. Clinical evaluation of the lesion is the key to differentiation, as some rare malignant entities may simulate benign lesions. A high index of suspicion should be maintained for any aggressive behavior, which may require more thorough evaluation, including histopathology and radiographic imaging studies. We report a rare case of cystic poorly differentiated squamous cell carcinoma (CPDSCC) of the scalp. Case presentation We report a case of a 37-year-old Filipino expatriate male who presented with a scalp swelling which had been gradually increasing in size for four months and was operated upon with a working diagnosis of sebaceous cyst. On post-op excisional biopsy, it turned out to be poorly differentiated cystic squamous cell carcinoma of the scalp. On further workup, no metastasis or other primary was found. Complete re-excision of the lesion with no evidence of residual tumor was achieved. Long-term follow-up was lost, as the patient left for his native country. Conclusion Though cystic cutaneous lesions are very commonly encountered in clinical practice, high suspicion for malignancy should be maintained if the lesion shows any aggressive behavior. Prompt investigation should be done before surgery to determine the nature of the disease and the most effective management for the patient. Poorly differentiated cystic squamous cell carcinoma should also be considered in the differential diagnosis of cystic cutaneous lesions show aggressive behavior.
机译:简介皮肤囊性病变的范围广泛,从常见的良性实体到罕见的恶性病变。病变的临床评估是分化的关键,因为一些罕见的恶性实体可能会模拟良性病变。对于任何侵略行为,都应保持高度怀疑,这可能需要进行更彻底的评估,包括组织病理学和射线照相成像研究。我们报告头皮囊性低分化鳞状细胞癌(CPDSCC)的罕见情况。病例介绍我们报告了一例37岁的菲律宾籍外籍男性,他的头皮肿胀逐渐增大,持续了四个月,并且经手术诊断为皮脂囊肿。手术后切除活检证实是头皮囊性鳞状细胞癌低分化。在进一步检查中,未发现转移或其他原发灶。完全切除病变,没有残留肿瘤的迹象。由于患者离开家乡,长期的随访失去了。结论尽管囊性皮肤病变在临床实践中很常见,但如果病变表现出任何侵略性行为,则应高度怀疑恶性肿瘤。手术前应及时进行调查,以确定疾病的性质以及对患者的最有效管理。分化差的囊性鳞状细胞癌在鉴别诊断中还应考虑囊性皮肤病变表现出侵袭性。

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