Park Ki-Ho, Lee Mi Suk, Hong Il Ki, Sung Ji-Youn, Choi Sang-Ho, Park Sang Ok, Shin Myung Jin, Chung Hye Won, Lee Sang Hoon
From the Departments of *Internal Medicine, †Nuclear Medicine, and ‡Pathology, Kyung Hee University Hospital, Kyung Hee University School of Medicine, Seoul Republic of Korea; and Departments of §Infectious Diseases and ¶Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Sex Transm Dis. 2014 Sep;41(9):532-7. doi: 10.1097/OLQ.0000000000000164.
Bone involvement is an unusual manifestation of secondary syphilis, but little information is available in the English-language literature. We carried out a systematic review of the English-language literature from 1964 to 2013, describing cases of secondary syphilis with bone involvement. We also describe a case of secondary syphilis with multiple osteolytic lesions, mimicking metastatic cancer or myeloma, which was included in an analysis of 37 eligible cases of secondary syphilis with bone involvement. Of these 37 patients, 28 (76%) patients were male, and the median age was 32 years (range, 12-64 years). Eleven (30%) patients had human immunodeficiency virus (HIV) infection with a median CD4 lymphocyte count of 343 cells/mm (range, 130-689 cells/mm). The diagnosis of early syphilis was suspected based on mucocutaneous findings in 28 (76%) cases. In the remaining 9 (24%) cases, high titers of nontreponemal serologic tests were the only evidence of early syphilis. The median venereal disease research laboratory (VDRL) titer was 1:64 (range, 1:8-1:320), and median rapid plasma reagin (RPR) titer was 1:64 (range, 1:16-1:512). The bones most often affected were long bones of the limbs (n = 22) and skull (n = 21). The bone lesions were multifocal in 27 (73%) cases and osteolytic in 19 (51%) cases. The treatment of syphilitic bone lesions was medical only in most patients, and prognosis was favorable with high-dose penicillin therapy. Clinical features and outcome between HIV-uninfected and HIV-infected patients were not different. Knowledge of this rare entity may lead to early diagnosis and appropriate management.
骨骼受累是二期梅毒的一种不常见表现,但英文文献中相关信息较少。我们对1964年至2013年的英文文献进行了系统综述,描述了伴有骨骼受累的二期梅毒病例。我们还描述了一例伴有多发溶骨性病变的二期梅毒病例,该病例类似转移性癌或骨髓瘤,此病例纳入了对37例符合条件的伴有骨骼受累的二期梅毒病例的分析。在这37例患者中,28例(76%)为男性,中位年龄为32岁(范围12 - 64岁)。11例(30%)患者感染了人类免疫缺陷病毒(HIV),CD4淋巴细胞计数中位数为343个细胞/mm³(范围130 - 689个细胞/mm³)。28例(76%)病例根据皮肤黏膜表现怀疑早期梅毒诊断。其余9例(24%)病例中,非梅毒螺旋体血清学检测高滴度是早期梅毒的唯一证据。性病研究实验室(VDRL)滴度中位数为1:64(范围1:8 - 1:320),快速血浆反应素(RPR)滴度中位数为1:64(范围1:16 - 1:512)。最常受累的骨骼是四肢长骨(n = 22)和颅骨(n = 21)。27例(73%)病例的骨病变为多灶性,19例(51%)病例为溶骨性。大多数患者梅毒骨病变仅采用药物治疗,大剂量青霉素治疗预后良好。未感染HIV和感染HIV患者的临床特征及结局无差异。了解这种罕见情况可能有助于早期诊断和恰当处理。