Malignant Epithelioid Neoplasm versus Dedifferentiated Malignant Melanoma: A Case Report.

IF 2.9 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Angela Rosenberg, Chapman Wei, Yisroel Grabie, Stephanie Chain, Sakura Thapa, Gita Vatandoust
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Abstract

The metastasis of poorly differentiated epithelioid carcinoma to the axillary node is uncommon. This tumor has heterogeneous expression and is challenging to diagnose with certainty. Often, it necessitates immunoperoxidase staining to ascertain the tumor lineage, and diagnosis is prolonged due to low suspicion. Herein, we present a case involving a 75-year-old male war veteran with a prior history of a gunshot wound complicated by colostomy that presented with an axillary mass, fecal and urinary incontinence, leg weakness, fevers, night sweats, and substantial weight loss. On admission, he had heightened leukocytosis (43K), anemia (hemoglobin 6.6), and thrombophilia (1000). This patient constantly picked at his back to remove recurrent "gun shrapnel" eruptions. An excisional biopsy of the axillary mass was performed for diagnosis and lymph node removal. Notably, after excision, there was marked improvement in the presenting symptoms. Diagnostic challenges arose due to the tumor cells' inconsistent immunohistochemical marker expression. The staining patterns alluded to metastatic melanoma. Yet, the tumor displayed epithelial characteristics, supported by an immunophenotypic marker pattern indicative of poorly differentiated carcinoma. This case underscores the morphological and immunoperoxidase staining similarities between poorly differentiated carcinoma and dedifferentiated tumors of varying origins. It illustrates the intricate nature of these malignant metastatic tumors and their overlapping manifestations, which requires provider awareness. The timely diagnosis of poorly differentiated epithelial carcinoma remains paramount to early treatment and improved prognosis. Therefore, in patients manifesting with an axillary mass, fecal and urinary incontinence, and B-symptoms, poorly differentiated epithelial carcinoma should be included in the differential diagnosis.

恶性上皮样肿瘤与分化型恶性黑色素瘤:一份病例报告。
分化不良的上皮样癌转移到腋窝结节的情况并不常见。这种肿瘤表现不一,很难确诊。通常需要通过免疫过氧化物酶染色才能确定肿瘤的系谱,而且由于怀疑度低,诊断时间也会延长。在此,我们介绍一例 75 岁男性退伍军人的病例,他曾有枪伤史,并发结肠造口术,表现为腋窝肿块、大小便失禁、腿部无力、发热、盗汗和体重大幅下降。入院时,他的白细胞增多(43K)、贫血(血红蛋白 6.6)和血栓性疾病(1000)。该患者经常抠背,以去除反复出现的 "枪弹片 "糜烂。为了确诊和切除淋巴结,对腋窝肿块进行了切除活检。值得注意的是,切除术后,患者的症状明显好转。由于肿瘤细胞的免疫组化标记物表达不一致,诊断面临挑战。染色模式显示为转移性黑色素瘤。然而,肿瘤显示出上皮特征,免疫表型标记物模式显示为分化不良癌。该病例强调了分化不良癌和不同来源的去分化肿瘤在形态学和免疫过氧化物酶染色方面的相似性。它说明了这些恶性转移性肿瘤错综复杂的性质及其重叠的表现,这需要提供者提高认识。及时诊断分化不良上皮癌仍是早期治疗和改善预后的关键。因此,对于表现为腋窝肿块、大小便失禁和B型症状的患者,应将分化不良上皮癌纳入鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.80
自引率
0.00%
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审稿时长
6 weeks
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