Cutaneous Rosai - Dorfman disease in a patient with late syphilis and cervical cancer - case report and a review of literature.

Q2 Medicine
Angelika Bielach-Bazyluk, Agnieszka B Serwin, Agata Pilaszewicz-Puza, Iwona Flisiak
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引用次数: 3

Abstract

Background: Cutaneous Rosai - Dorfman disease (CRDD) is extremely rare variant of idiopathic histiocytic proliferative disorder, which may manifest as a non-specific macules, papules, plaques or nodules ranging in size and colour from yellow - red to red -brown.

Case presentation: A 52-year-old female presented with three gradually enlarging, reddish - brown nodules on the right upper extremity lasting six months. The patients denied fever, weight loss, malaise. Clinical examination and imaging tests showed no sign of lymphadenopathy. A biopsy specimen of a nodule showed a dense dermal polymorphic infiltrate with numerous histiocytes exhibiting emperipolesis phenomenon. Immunohistochemical staining of the histiocytes showed S-100 protein (+), CD68(+), but CD1a (-). Aforementioned findings were consistent with CRDD characteristics. Additionally, a routine serological screening and confirmatory serological tests for syphilis were positive. Syphilis of unknown duration was diagnosed. The IgG antibodies titre against Chlamydia trachomatis was elevated. An isolated sensory impairment over the right trigeminal nerve was found on neurological consultation. Comprehensive gynaecological assessment was carried out because of patient's complaints of bleeding after sexual intercourse and led to diagnosis of cervical cancer. The initial therapy with methotrexate was discontinued after three months due to neutropenia. Further therapy with dapson was ineffective, therefore complete surgical excision was recommended.

Conclusions: CRDD is a rare, benign condition especially difficult to diagnose due to lack of general symptoms and lymphadenopathy. Histopathologic examination with immunohistochemical staining, exhibiting characteristic and reproducible findings play a key role in establishing an accurate diagnosis. In the presented case activated histiocytes demonstrated in a lesional skin might be a response to immune dysregulation related to chronic, untreated sexually transmitted infections and cancer.

Abstract Image

Abstract Image

皮肤Rosai - Dorfman病并发晚期梅毒和宫颈癌1例报告并文献复习。
背景:皮肤Rosai - Dorfman病(CRDD)是一种非常罕见的特发性组织细胞增殖性疾病,可表现为非特异性斑点、丘疹、斑块或结节,其大小和颜色从黄红色到红棕色不等。病例介绍:一名52岁女性,右上肢出现3个逐渐增大的红棕色结节,持续6个月。病人否认发烧,体重减轻,不适。临床检查及影像学检查未见淋巴结病变征象。结节的活检标本显示密集的真皮多形性浸润,伴有大量组织细胞,表现为表皮增生现象。组织细胞免疫组化染色显示S-100蛋白(+),CD68蛋白(+),CD1a蛋白(-)。上述发现与CRDD特征一致。此外,常规血清学筛查和梅毒确认血清学试验均为阳性。诊断为持续时间不详的梅毒。沙眼衣原体IgG抗体滴度升高。在神经科会诊中发现了右三叉神经的孤立感觉障碍。由于患者主诉性交后出血,进行了全面的妇科评估,并诊断为宫颈癌。最初的甲氨蝶呤治疗在3个月后因中性粒细胞减少而停止。进一步应用氨苯砜治疗无效,因此建议完全手术切除。结论:CRDD是一种罕见的良性疾病,由于缺乏一般症状和淋巴结病变,尤其难以诊断。组织病理学检查与免疫组织化学染色,显示特征性和可重复的发现,在建立准确的诊断中发挥关键作用。在本病例中,病变皮肤中出现的活化组织细胞可能是对慢性、未经治疗的性传播感染和癌症相关的免疫失调的反应。
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来源期刊
BMC Dermatology
BMC Dermatology Medicine-Dermatology
自引率
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期刊介绍: BMC Dermatology is an open access journal publishing original peer-reviewed research articles in all aspects of the prevention, diagnosis and management of skin disorders, as well as related molecular genetics, pathophysiology, and epidemiology. BMC Dermatology (ISSN 1471-5945) is indexed/tracked/covered by PubMed, MEDLINE, CAS, EMBASE, Scopus and Google Scholar.
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