López Pérez Ricardo A, Sauza Gonzalez Victoria, Acuña Rocha Victor D, Fischer Rouyer Anette, Villapudua Torres Ashley Lilian, Franco Márquez Rodolfo
Internal Medicine, Hospital Universitario "Dr. José Eleuterio González", Monterrey, MEX.
Pathology, Hospital Universitario "Dr. José Eleuterio González", Monterrey, MEX.
Cureus. 2024 Oct 31;16(10):e72756. doi: 10.7759/cureus.72756. eCollection 2024 Oct.
Syphilis, caused by the spirochete , is a sexually transmitted infection (STI) that has seen a resurgence worldwide, particularly among populations at a higher risk of co-infection with human immunodeficiency virus (HIV). The disease typically progresses through distinct stages: primary, secondary, latent, and tertiary, each with specific clinical manifestations. Secondary syphilis is characterized by systemic involvement and various mucocutaneous symptoms, including a maculopapular rash that frequently involves the palms and soles along with fever, lymphadenopathy, and mucous membrane lesions. However, in patients with HIV co-infection, syphilis may present atypically. The immunosuppression caused by HIV can lead to more severe, atypical, and persistent manifestations of secondary syphilis. Furthermore, the cutaneous features may deviate from the classic presentation, making diagnosis challenging. We report the case of a male in his third decade of life, recently diagnosed with HIV, who presented with diffuse hyperpigmented dermatosis. The unusual presentation, including well-defined brown macules with a generalized distribution, initially raised suspicion for Kaposi's sarcoma (KS), a frequent cutaneous malignancy seen in HIV patients. Skin biopsy showed a dense perivascular and interstitial inflammatory infiltrate with marked endothelial swelling and vascular proliferation. Immunohistochemistry confirmed the presence of spirochetes, and a positive Venereal Disease Research Laboratory (VDRL) test further supported the diagnosis of secondary syphilis in the context of HIV. Our case underscores the importance of considering secondary syphilis in the differential diagnosis in cases of generalized hyperpigmented dermatosis in newly diagnosed HIV patients, where common conditions such as Kaposi's sarcoma may obscure the underlying etiology.
梅毒由螺旋体引起,是一种性传播感染(STI),在全球范围内呈回升趋势,尤其是在合并感染人类免疫缺陷病毒(HIV)风险较高的人群中。该疾病通常经历不同阶段:一期、二期、潜伏期和三期,每个阶段都有特定的临床表现。二期梅毒的特征是全身受累以及各种皮肤黏膜症状,包括经常累及手掌和足底的斑丘疹,同时伴有发热、淋巴结病和黏膜损害。然而,在合并感染HIV的患者中,梅毒可能表现不典型。HIV引起的免疫抑制可导致二期梅毒出现更严重、不典型和持续的表现。此外,皮肤特征可能偏离经典表现,使诊断具有挑战性。我们报告了一例30岁男性病例,该患者最近被诊断为HIV感染,表现为弥漫性色素沉着性皮肤病。这种不寻常的表现,包括边界清晰、广泛分布的褐色斑疹,最初引发了对卡波西肉瘤(KS)的怀疑,KS是HIV患者中常见的皮肤恶性肿瘤。皮肤活检显示密集的血管周围和间质炎症浸润,伴有明显的内皮肿胀和血管增生。免疫组织化学证实存在螺旋体,性病研究实验室(VDRL)试验阳性进一步支持了在HIV背景下二期梅毒的诊断。我们的病例强调了在新诊断的HIV患者出现全身性色素沉着性皮肤病的鉴别诊断中考虑二期梅毒的重要性,因为卡波西肉瘤等常见疾病可能掩盖潜在病因。