长期未确诊的典型卡波西肉瘤伴大面积皮肤疹1例。

IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL
JMA journal Pub Date : 2025-04-28 Epub Date: 2025-01-31 DOI:10.31662/jmaj.2024-0161
Kouhei Takehara, Yasuhito Hamaguchi, Kou Fujii, Motoki Horii, Natsumi Fushida, Tasuku Kitano, Shintaro Maeda, Kyosuke Oishi, Katsushige Taniuchi, Takashi Matsushita
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引用次数: 0

摘要

卡波西肉瘤(KS)是一种慢性多灶性淋巴血管增生性肿瘤,主要发生在地中海地区的老年人中。在获得性免疫缺陷综合征患者中,KS常被视为一种恶性肿瘤,典型的KS是罕见的。一位82岁男性患者因双侧下肢水肿伴紫癜及小结节而转诊至我科。患者50多岁时,下肢出现水肿伴紫癜,无特殊诱因。8年前(70多岁),紫癜病变逐渐变成结节状。两年前,他的前臂和手背也出现了类似的皮疹。体格检查显示整个下肢弥漫性棕色凹陷性水肿,从双侧手背一直延伸到肘部。多发性紫红色,弹性,硬结节,范围从几毫米到约1厘米,局限并融合在水肿上。前臂结节的组织学检查显示胶原纤维增生和真皮细胞浸润。真皮内错综复杂的增殖细胞呈梭形,细胞核圆形。免疫组化染色显示梭形细胞CD31、CD34和D2-40阳性。这些细胞对人类疱疹病毒(HHV)-8呈阳性,对人类免疫缺陷病毒(HIV)抗原和抗体呈阴性。他被诊断为典型的KS。我们建议化疗,但他拒绝接受任何治疗。我们的病人没有接受任何免疫抑制治疗,HIV检测结果为阴性。因此,免疫抑制状态可能与我们患者的KS发展无关。他有机会咨询皮肤科医生,但从未被诊断为KS。皮肤活检有助于诊断KS;因此,当患者出现长期、缓慢进展、不明原因的腿部水肿并伴有皮疹时,应予以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of Long-undiagnosed Classic Kaposi's Sarcoma with Extensive Skin Eruptions.

Kaposi's sarcoma (KS) is a chronic, multifocal lymphoangioproliferative tumor that occurs mainly in older individuals in the Mediterranean region. KS is often observed as a malignant tumor in patients with acquired immunodeficiency syndrome, and classic KS is rare. An 82-year-old man was referred to our department with bilateral lower-leg edema with purpura and small nodules. When the patient was in his mid-50s, edema with purpura appeared in his lower extremities without any specific trigger. Eight years earlier (in his mid-70s), the purpura lesions gradually turned nodular. A similar skin rash appeared on the forearms and back of the hands two years earlier. Physical examination revealed diffuse brown pitting edema over the entirety of the lower extremities and extending from the dorsum of the bilateral hands to the elbows. Multiple purple-red, elastic, hard nodules ranging from a few millimeters to about 1 cm were localized and fused over the edema. Histological examination of the forearm nodule revealed proliferation of collagen fibers and cellular infiltration in the dermis. The intricately proliferating cells in the dermis were spindle-shaped with round nuclei. Immunohistochemical staining revealed spindle-shaped cells positive for CD31, CD34, and D2-40. These cells were positive for human herpesvirus (HHV)-8 and negative for human immunodeficiency virus (HIV) antigens and antibodies. He was diagnosed with classic KS. We proposed chemotherapy, but he refused to receive any treatment. Our patient did not receive any immunosuppressive therapy, and the HIV test result was negative. Therefore, immunosuppressive status may not be involved in the development of KS in our patient. He had opportunities to consult dermatologists but was never diagnosed with KS. A skin biopsy helps diagnose KS; thus it should be considered when a patient experiences long-standing, slowly progressive, unexplained leg edema accompanied by a skin rash.

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