Department of Dermatology and Venereology, Medical University of Bialystok, Białystok, Poland.
Department of Medical Pathomorphology, Medical University of Bialystok, Białystok, Poland.
BMC Dermatol. 2020 Dec 7;20(1):19. doi: 10.1186/s12895-020-00115-w.
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.
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.
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.
皮肤 Rosai-Dorfman 病(CRDD)是一种罕见的特发性组织细胞增生性疾病的变体,其表现为大小和颜色从黄色到红棕色不等的非特异性斑疹、丘疹、斑块或结节。
一名 52 岁女性,右侧上肢有三个逐渐增大的红色棕色结节,持续了六个月。患者否认发热、体重减轻、不适。临床检查和影像学检查均未显示淋巴结病迹象。结节的活检标本显示出密集的真皮多形性浸润,其中许多组织细胞表现出 emperipolesis 现象。组织细胞的免疫组织化学染色显示 S-100 蛋白(+),CD68(+),但 CD1a(-)。上述发现与 CRDD 的特征一致。此外,梅毒的常规血清学筛查和确证性血清学检查均为阳性。诊断为原因不明的梅毒。针对沙眼衣原体的 IgG 抗体滴度升高。神经科会诊发现右侧三叉神经感觉障碍。由于患者有性交后出血的主诉,因此进行了全面的妇科评估,导致诊断为宫颈癌。由于中性粒细胞减少,甲氨蝶呤的初始治疗在三个月后停止。进一步的磺胺嘧啶治疗无效,因此建议进行完全手术切除。
CRDD 是一种罕见的良性疾病,由于缺乏一般症状和淋巴结病,尤其难以诊断。具有特征性和可重复性发现的组织病理学检查结合免疫组织化学染色在确立准确诊断中起着关键作用。在本例中,病变皮肤中激活的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免疫失调的反应。