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二期梅毒的不寻常表现:病例报告

Unusual Manifestations of Secondary Syphilis: Case Presentations.

作者信息

Dănescu Sorina Ana, Szolga Blanca, Georgiu Carmen, Surcel Alina, Corina Șenilă Simona Corina

机构信息

Sorina Ana Dănescu, MD, University of Medicine and Pharmacy "Iuliu Hatieganu", Victor Babes 8 street, Cluj-Napoca, Cluj, Romania;

出版信息

Acta Dermatovenerol Croat. 2018 Jun;26(2):186-188.

Abstract

Dear Editor, Syphilis is an infection caused by Treponema pallidum. Without treatment, it goes through the following stages: primary, secondary, latent, and tertiary (1). The clinical picture of secondary syphilis is very variable (2,3). We present two rare cases of secondary syphilis, one with nodular lesions initially considered to be lymphoma and second with periostitis, which was initially interpreted as an osteoma. To date, only 15 cases with nodular lesions and 10 cases with periostitis in secondary syphilis have been reported in the literature. The first patient was a 59 year old man who presented in a private practice with nodular lesions on the face and axillary and inguinal folds (Figure 1, a, b). The initial diagnostic consideration was lymphoma. A biopsy specimen was taken, and the histopathological features revealed epidermal hyperplasia with papillomatosis, minimal spongiosis with many neutrophils and with a marked inflammatory infiltrate in dermis, consisting of lymphocytes, plasma cells, and neutrophils; the diagnosis of interfaced dermatitis was established (Figure 1, d, e). After one month, the patient presented to our clinic with numerous nodular lesions, some of them painful, located on the trunk and intertriginous folds, including the intergluteal cleft - the lesions in this area being suggestive of condylomata lata (Figure 1, c). The diagnosis of secondary syphilis was taken into consideration, and screening serum tests were performed and found reactive: a Venereal Diseases Research Laboratory (VDRL) titer of 1:64 and Treponema pallidum Hemaglutination Assay (TPHA) titer of 1:80. Hepatitis and anti-human immunodeficiency virus (HIV) antibodies serology was negative. The biopsy was repeated and showed the same histopathological changes. In addition, Warthin-Starry staining was performed, revealing the presence of some spiral micro-organisms in the dermis corresponding to Treponema pallidum (Figure 1, f). A diagnosis of secondary syphilis was established, and the patient was treated with benzathine penicillin G 2.4 million units by intramuscular injection once a week for 2 consecutive weeks. The skin lesions regressed within 1 month, and serological tests showed a VDRL titer of 1:8 3 months after treatment. The second patient was a homosexual male, 35 years old, diagnosed with HIV infection, stage B2. He presented with bone pain in the calves and forearms, with insidious onset. He also presented with an associated erythematous maculo-papular rash on the trunk and limbs and generalized lymphadenopathy (Figure 2, a, b). The tibial crest and radius were sensitive to palpation. A right leg radiography was performed, raising suspicion of osteoid osteoma. The CT scan excluded the diagnosis of osteoma; taking into account the epidemiological context, the diagnosis of syphilis was suspected. The diagnosis was confirmed by leg ultrasound examination (2D US) which showed thickening of the compact tibial bone associated with subperiosteal destructive and proliferative changes (Figure 2, c, d) and by serology for syphilis: the VDRL titer was 1:32 and the TPHA titer was 1:80. The patient was treated with benzathine penicillin 2.4 million units, once a week, for 2 consecutive weeks, with clinical improvement. Syphilis continues to be a serious public health problem worldwide, even if it is a controllable disease due to diagnostic tests and effective and accessible treatment. According to the World Health Organization in 2008, the estimated number of new cases of sexually transmitted diseases in adults with syphilis is 10.6 million cases (4). The cases presented in this paper were characterized by unusual manifestations, requiring good collaboration between the dermatologist and other specialties. In the first case, the diagnosis of secondary syphilis was confirmed by positive serological, clinical, and histopathological findings. The main differential diagnosis of nodular syphilis includes lymphoma, sarcoidosis, Kaposi's sarcoma, atypical mycobacteriosis, deep fungal infections, leprosy, tuberculosis, leishmaniasis, and lymphomatoid papulosis (5). Another important differential diagnosis is between secondary and tertiary syphilis, especially when ulcerating nodules are present. Tertiary syphilis is characterized by unilateral, deep ulcerating nodules with necrotizing granulomas (6). Bone involvement during syphilis is mainly represented by polyarthritis, synovitis, osteitis, and periostitis (7,8). Syphilitic periostitis is characterized by localized or diffuse pain, particularly during the night, which is relieved by movement. The skull, the shoulder girdle, and the long bones are the most common sites of involvement (9). In conclusion, we presented two different cases of secondary syphilis that contribute to the clinical experience of rare cases presented in the literature, raising the awareness of dermatologists and other specialists about less specific clinical aspects of syphilis.

摘要

尊敬的编辑,梅毒是由梅毒螺旋体引起的一种感染性疾病。若不进行治疗,它会经历以下几个阶段:一期、二期、潜伏期和三期(1)。二期梅毒的临床表现非常多样(2,3)。我们在此呈现两例罕见的二期梅毒病例,一例表现为结节性病变,最初被误诊为淋巴瘤;另一例表现为骨膜炎,最初被误诊为骨瘤。迄今为止,文献中仅报道了15例二期梅毒伴有结节性病变的病例以及10例伴有骨膜炎的病例。

首例患者为一名59岁男性,因面部、腋窝及腹股沟褶皱处出现结节性病变前来私人诊所就诊(图1,a、b)。初步诊断考虑为淋巴瘤。遂取活检标本,组织病理学特征显示表皮增生伴乳头瘤样变,轻度海绵形成,有许多中性粒细胞,真皮层有明显的炎症浸润,由淋巴细胞、浆细胞和中性粒细胞组成;确诊为界面性皮炎(图1,d、e)。一个月后,该患者前来我院就诊,躯干及间擦部位出现大量结节性病变,其中一些伴有疼痛,包括臀间裂处的病变,此区域病变提示扁平湿疣(图1,c)。考虑二期梅毒的诊断,进行了血清学筛查,结果呈阳性:性病研究实验室(VDRL)滴度为l:64,梅毒螺旋体血凝试验(TPHA)滴度为l:80。肝炎及抗人类免疫缺陷病毒(HIV)抗体血清学检查均为阴性。再次活检显示相同的组织病理学改变。此外,进行了Warthin-Starry染色检查,结果显示真皮层存在一些螺旋状微生物,符合梅毒螺旋体特征(图1,f)。确诊为二期梅毒,给予患者苄星青霉素G 240万单位,肌肉注射,每周1次,连续2周。皮肤病变在1个月内消退,治疗3个月后血清学检查显示VDRL滴度为l:8。

第二例患者为一名35岁男性同性恋者,诊断为HIV感染,B2期。他因小腿和前臂隐匿性骨痛前来就诊。同时,他还伴有躯干和四肢的红斑丘疹性皮疹及全身淋巴结肿大(图2,a、b)。胫骨嵴和桡骨压痛明显。行右腿X线检查,怀疑为骨样骨瘤。CT扫描排除了骨瘤诊断;结合流行病学背景,怀疑梅毒诊断。腿部超声检查(二维超声)证实了诊断,显示胫骨皮质增厚,伴有骨膜下破坏和增生性改变(图2,c、d),梅毒血清学检查结果为:VDRL滴度为l:32,TPHA滴度为l:80。给予患者苄星青霉素240万单位,每周1次,连续2周,临床症状改善。

梅毒在全球范围内仍然是一个严重的公共卫生问题,尽管由于诊断检测以及有效且可及的治疗手段,它是一种可控制的疾病。根据世界卫生组织2008年的数据,成人梅毒新发病例估计达1060万例(4)。本文所呈现的病例具有不寻常的表现,需要皮肤科医生与其他专科之间良好协作。在首例病例中,二期梅毒的诊断通过血清学、临床及组织病理学检查结果呈阳性得以证实。结节性梅毒的主要鉴别诊断包括淋巴瘤、结节病、卡波西肉瘤、非典型分枝杆菌病、深部真菌感染、麻风、结核、利什曼病以及淋巴瘤样丘疹病(5)。另一个重要的鉴别诊断是二期梅毒与三期梅毒之间的鉴别,尤其是当出现溃疡性结节时。三期梅毒的特征为单侧、深部溃疡性结节伴坏死性肉芽肿(6)。梅毒累及骨骼主要表现为多关节炎、滑膜炎、骨炎和骨膜炎(7,8)。梅毒性骨膜炎的特征为局部或弥漫性疼痛,尤其是在夜间,活动后可缓解。颅骨、肩胛带及长骨是最常受累的部位(9)。

总之,我们呈现了两例不同的二期梅毒病例,丰富了文献中罕见病例的临床经验,提高了皮肤科医生及其他专科医生对梅毒不太典型临床症状的认识。

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