梅格斯综合征、假梅格斯综合征还是假-假梅格斯综合征?病例报告

Azie Jumaatul Adawiyah Nabir , Chiew Yee Lau , Adilah W. Ab Rahim , Aliyyah Mohammad Khuzaini
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引用次数: 0

摘要

病例报告我们报告了一例 6 岁女孩的病例,她出现进行性呼吸困难、嗜睡和便秘两周,伴有多次发作的关节疼痛和多形性皮疹。胸部、腹部和盆腔影像学检查提示双侧胸腔积液、腹水和腹部受累的卵巢肿块。胸腔和腹腔积液呈渗出性。不幸的是,她不适合对肿块进行活检,因此在重症监护室接受了一个月的治疗。由于怀疑有潜在的自身炎症,她开始口服皮质类固醇。然而,随后的检查并没有得出结论。她逐渐康复,并在一年后恢复健康。她再次出现全身症状,被诊断为弥漫大 B 细胞淋巴瘤(DLBCL)。结论我们描述了一个症状暂时缓解的 DLBCL 异常表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Meigs syndrome, pseudo-Meigs syndrome, or pseudo-pseudo Meigs syndrome? A case report

Background

Meigs syndrome, pseudo-Meigs syndrome, and pseudo-pseudo-Meigs syndrome showcase a diagnostic challenge in the management of complex pediatric cases.

Case report

We report a case of a 6-year-old girl who presented with progressive breathlessness, lethargy, and constipation for two weeks, associated with multiple episodes of joint pain and polymorphous rash. Imaging of the thorax, abdomen, and pelvis suggested bilateral pleural effusion, ascites, and an ovarian mass with abdominal involvement. The pleural and peritoneal fluids were exudative in nature. Unfortunately, she was not fit for a biopsy of the mass and was treated in the intensive care unit for one month. She was initiated on oral corticosteroids for suspicion of an underlying auto-inflammatory disease. However, subsequent investigations yielded inconclusive results. She gradually recovered and was well for a year. She presented again with constitutional symptoms and was diagnosed with diffuse large B-cell lymphoma (DLBCL). Thus, it was retrospectively apparent that this was a case of pseudo-Meigs syndrome.

Conclusion

We describe an unusual presentation of DLBCL with a temporary resolution of symptoms.
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