青少年血管肌瘤错构瘤伪装成淋巴细胞增生性疾病

Kamila Askarova , Malika Shukurova , Shaxnoz Mamadjanova
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引用次数: 0

摘要

背景:腹股沟淋巴结错构瘤(AMH-LN)是一种少见的平滑肌、血管、胶原基质和脂肪细胞的良性增生,最常见于腹股沟淋巴结(LN)。病例报告我们报告了一位16岁的男性,他最初因双侧腹股沟淋巴结病来就诊。组织学评估提示诊断为非霍奇金淋巴瘤,而免疫组织化学分析显示与Castleman病一致的结果。然而,进一步的综合成像、反复的组织病理学检查和免疫组织化学研究最终显示了一个意想不到的淋巴结血管肌瘤性错构瘤(AMH)的诊断。结论该病例强调了多学科综合治疗的必要性,以避免儿童和青少年淋巴结病的误诊和不必要的干预。这种罕见的良性疾病强调了在诊断或排除恶性肿瘤时仔细的组织学评估的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Angiomyomatous hamartoma masquerading as lymphoproliferative disease in a teenager

Background

Angiomyomatous hamartoma of lymph nodes (AMH-LN) is an uncommon benign proliferation of smooth muscle, blood vessels, collagenous stroma, and adipocytes, most commonly affecting inguinal lymph nodes (LN). [1]

Case report

We present a 16-year-old male who initially came to us with bilateral inguinal lymphadenopathy. Histological evaluation suggested a diagnosis of non-Hodgkin lymphoma, while immunohistochemical analysis indicated findings consistent with Castleman disease. However, further comprehensive imaging, repeated histopathological examination, and immunohistochemical studies ultimately revealed an unexpected diagnosis of angiomyomatous hamartoma (AMH) of the lymph nodes.

Conclusion

The case underscores the necessity of multidisciplinary approache to avoid misdiagnosis and unnecessary interventions in pediatric and adolescent patients presenting with lymphadenopathy. This rare benign condition highlighted the importance of careful histological evaluation in diagnosing or ruling out malignancies.
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