Toberer Ferdinand, Hanner Susanne, Haus Georg, Haenssle Holger A
Ferdinand Toberer, MD, Department of Dermatology, Venerology and Allergology, University Medical Center, Ruprecht-Karls-University, Im Neuenheimer Feld, 69120 Heidelberg, Germany;
Acta Dermatovenerol Croat. 2019 Sep;27(3):190-191.
A 35-year-old Caucasian woman, otherwise healthy, presented with a four weeks history of painful, inflammatory nodules, each with a central opening on her right lower leg (Figure 1). Intermittently, a marked serosanguinous secretion was noted. The remaining skin and mucosa were not affected. The patient denied any history of trauma. One month earlier she had returned from a journey to Peru. Despite topical treatment with corticosteroids and antibiotics as well as systemic therapy with oral doxycycline, the lesions did not show any regression or reduction in their secretion. An incisional biopsy was performed at all sites and the extracted organic specimens were submitted for histopathological assessment. Histopathology revealed a mixed inflammatory dermal infiltrate consisting of numerous eosinophils admixed with some histiocytes and lymphocytes. Furthermore, an organic foreign body with an eosinophilic cuticle consistent with DH became evident (Figure 2, a-e). Human myiasis represents the infestation of humans by developing dipterous larvae (maggots) of various fly species (1). The most common flies causing human myiasis are Dermatobia hominis (DH, "human botfly") and, less frequently, Cordylobia anthropophaga ("tumbu fly") or Cordylobia rodhaini (1). DH is indigenous in Central and South America, but in Europe and the United States of America only cases of travelers that imported the infestation have been described (2,3). The adult DH is a yellow-headed fly with a grey-blue body of approximately 15 mm. DH is active throughout the year and predominantly found in humid and high temperature regions of Central and South America (2). The larvae of DH develop as obligate parasites in living tissue, causing furuncular myiasis (2,4). Clinically crusted nodules with serosanguinous secretion and sometimes nocturnal pain affecting uncovered anatomical sites are typical (2,4). Differential diagnoses include bacterial furunculosis, arthropod bite reaction, pyoderma, inflamed epidermoid cysts, or cutaneous leishmaniasis (2,5-7). Most cases of furuncular myiasis can be diagnosed solely by their clinical presentation and after carefully taking the patients' history. Nevertheless, dermoscopy and sonography may help to confirm the diagnosis and rule out the abovementioned differential diagnoses (6,7). Although myiasis is a self-limited disease, it can be accompanied by severe complications including tetanus or bacterial superinfections (2). The literature reports a number of treatment options including a) occlusion of the skin opening by paraffin oil, beeswax, petroleum jelly or agents such as liquid nitrogen or ethyl chloride sprays to suffocate the larva and promote self-extrusion; b) removing the larva by forceps after lidocaine instillation; c) surgical removal or d) the use of topical or oral ivermectin (1,8,9). Preventive measures include protective clothing, insect repellents, and sleeping curtains. Histopathology of furuncular myiasis typically reveals a mixed inflammatory infiltrate of eosinophils, lymphocytes, and macrophages. Sometimes formation of granulomas with giant cells becomes evident (10). Fly larvae show a thick eosinophilic cuticle with external facing sclerotized spines. Internal structures (respiratory and digestive tracts or striated muscle) may occasionally be identified (10), (Figure 2, b-e). In most cases, tissue sections will not be sufficient to identify the fly's genus or its species; however, identification by stereomicroscopy has been reported (10). In conclusion, we described the clinical and histopathological features of furuncular myiasis by DH in a traveler returning from Peru. Given the ever-increasing numbers of international travelers, western dermatopathologists and dermatologists should be familiar with this disease to avoid prescription of unnecessary topical or systemic medications.
一名35岁的白种女性,身体健康,右小腿出现疼痛性炎性结节4周,每个结节中央有一个开口(图1)。间歇性地,可见明显的浆液性血性分泌物。其余皮肤和黏膜未受影响。患者否认有任何外伤史。一个月前她从秘鲁旅行归来。尽管使用了皮质类固醇和抗生素进行局部治疗以及口服强力霉素进行全身治疗,但病变并未出现任何消退或分泌物减少的情况。在所有部位进行了切开活检,并将提取的组织标本送去进行组织病理学评估。组织病理学显示真皮混合性炎性浸润,由大量嗜酸性粒细胞与一些组织细胞和淋巴细胞混合组成。此外,可见一个具有嗜酸性角质层的有机异物,符合人肤蝇感染(图2,a - e)。人肤蝇病是指人体被各种蝇类的发育中的双翅目幼虫(蛆)寄生(1)。引起人肤蝇病最常见的蝇类是人皮蝇(DH,“人肤蝇”),较少见的是嗜人瘤蝇(“穿皮潜蝇”)或罗氏瘤蝇(1)。人皮蝇原产于中美洲和南美洲,但在欧洲和美国,仅报道过输入性感染的旅行者病例(2,3)。成年人皮蝇是一种头部黄色、身体灰蓝色、体长约15毫米的蝇类。人皮蝇全年活动,主要分布在中美洲和南美洲的潮湿高温地区(2)。人皮蝇的幼虫在活体组织中作为专性寄生虫发育,引起疖肿性蝇蛆病(2,4)。临床上典型表现为有浆液性血性分泌物的结痂结节,有时夜间疼痛,累及未覆盖的解剖部位(2,4)。鉴别诊断包括细菌性疖病、节肢动物叮咬反应、脓疱病、炎性表皮样囊肿或皮肤利什曼病(2,5 - 7)。大多数疖肿性蝇蛆病病例仅通过临床表现及仔细询问患者病史即可诊断。然而,皮肤镜检查和超声检查可能有助于确诊并排除上述鉴别诊断(6,7)。尽管蝇蛆病是一种自限性疾病,但可能伴有严重并发症,包括破伤风或细菌超级感染(2)。文献报道了多种治疗方法,包括:a)用石蜡油、蜂蜡、凡士林或液氮或氯乙烷喷雾剂等药物封闭皮肤开口,使幼虫窒息并促进自行排出;b)在注射利多卡因后用镊子取出幼虫;c)手术切除;或d)使用局部或口服伊维菌素(1,8,9)。预防措施包括防护服、驱虫剂和蚊帐。疖肿性蝇蛆病的组织病理学通常显示嗜酸性粒细胞、淋巴细胞和巨噬细胞的混合性炎性浸润。有时可见形成有巨细胞的肉芽肿(10)。蝇蛆显示有一层厚厚的嗜酸性角质层,其外表面有硬化的棘。偶尔可识别内部结构(呼吸道、消化道或横纹肌)(10),(图2,b - e)。在大多数情况下,组织切片不足以识别蝇的属或种;然而,已有通过体视显微镜进行识别的报道(10)。总之,我们描述了一名从秘鲁归来的旅行者因人皮蝇引起的疖肿性蝇蛆病的临床和组织病理学特征。鉴于国际旅行者数量不断增加,西方皮肤病理学家和皮肤科医生应熟悉这种疾病,以避免开具不必要的局部或全身用药处方。