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酷似腺癌的直肠原发性无黑色素性黑色素瘤。

Primary amelanotic melanoma of the rectum mimicking adenocarcinoma.

作者信息

Sahoo Manash Ranjan, Gowda Manoj Srinivas, Kaladagi Raghavendra Mohan

机构信息

Department of Surgery, SCB Medical College and Hospital, Cuttack, Odisha, India.

出版信息

Am J Case Rep. 2013 Jul 26;14:280-3. doi: 10.12659/AJCR.889089. Print 2013.

Abstract

PATIENT

Male, 55 FINAL DIAGNOSIS: Melanoma Symptoms: Worsening constipation • tenesmus • weight loss

MEDICATION

  • Clinical Procedure: Chemoradiation therapy Specialty: Oncology.

OBJECTIVE

Challenging differential diagnosis.

BACKGROUND

Malignant melanoma is usually readily diagnosed by the presence of melanin granules. Although amelanotic melanoma contains a few melanin granules, it is often difficult to differentiate from non-epithelial malignant tumors. Immunohistochemical staining may be needed to diagnose the condition.

CASE REPORT

This report describes a case of amelanotic melanoma of the rectum, which was originally suspected to be an adenocarcinoma, but was subsequently correctly diagnosed by immunohistochemical staining with HMB-45 antibody and by the presence of S-100 protein. A pinkish-red ulceroproliferative growth was located about 7 cm from the anal verge. The patient was treated by laparoscopic low anterior resection.

CONCLUSIONS

Very few cases of amelanotic melanoma of rectum have been reported in the literature and there is only limited clinical experience with this disease. It appears to be a highly lethal tumor and may need much more aggressive treatment than that used for carcinoma of the rectum.

摘要

患者

男性,55岁 最终诊断:黑色素瘤 症状:便秘加重、里急后重、体重减轻

用药情况

  • 临床操作:放化疗 专业:肿瘤学

目的

具有挑战性的鉴别诊断

背景

恶性黑色素瘤通常通过黑色素颗粒的存在容易诊断。尽管无黑色素性黑色素瘤含有少量黑色素颗粒,但通常难以与非上皮性恶性肿瘤区分开来。可能需要免疫组化染色来诊断该疾病。

病例报告

本报告描述了一例直肠无黑色素性黑色素瘤病例,最初怀疑为腺癌,但随后通过HMB - 45抗体免疫组化染色及S - 100蛋白的存在得以正确诊断。一个粉红色的溃疡增生性肿物位于距肛缘约7厘米处。患者接受了腹腔镜低位前切除术治疗。

结论

文献中报道的直肠无黑色素性黑色素瘤病例极少,对此疾病的临床经验有限。它似乎是一种高度致命的肿瘤,可能需要比直肠癌更积极的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9da/3731173/a401e08b7720/amjcaserep-14-280-g001.jpg

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