Kakurai Masakazu, Iwamoto Kazuma, Moriyama Yoshihiro
Dermatology, Tsuchiura Kyodo General Hospital, Tsuchiura, JPN.
Cureus. 2025 May 3;17(5):e83427. doi: 10.7759/cureus.83427. eCollection 2025 May.
Rheumatoid neutrophilic dermatosis (RND) is associated with rheumatoid arthritis and typically presents as papules, nodules, and/or plaques bilaterally on the extremities. Rarely, vesiculobullous lesions (bullous RND) may occur. We herein present a case of bullous RND diagnosed in our department. A 70-year-old Japanese woman presented with multiple painful, tense bullae, accompanied by pustules, erythematous papules, and erosions on the lower extremities, and a few hemorrhagic bullae were observed on the soles. Her medical history included seropositive rheumatoid arthritis for 14 years, which was successfully treated with oral prednisolone and tacrolimus hydrate, but joint pain and swelling developed one month before her visit to our department. A skin biopsy of the blister on the lower leg revealed an intraepidermal and subepidermal blister, containing numerous neutrophils. Marked neutrophilic infiltration, showing prominent leukocytoclasis, was observed in the dermis without vasculitis. Direct immunofluorescence yielded negative results. Bacterial cultures from the blisters were sterile. Taken together, the diagnosis of bullous RND was made. Despite treatment with oral minocycline for one week, new skin lesions developed. Treatment was switched to dapsone at 75 mg daily, resulting in the improvement of skin lesions and arthralgia within one week. In this report, we describe a case of bullous RND and compare the differences in clinical findings between bullous and non-bullous RND, which have not been previously documented. Additionally, as RND and Sweet's syndrome share overlapping clinicopathological features, we proposed five diagnostic criteria for RND: (1) a definitive diagnosis of rheumatoid arthritis; (2) high rheumatoid arthritis disease activity; (3) multiple erythematous papules, nodules, plaques, and/or tense vesiculobullous lesions; (4) predominantly neutrophilic dermal infiltrate without leukocytoclastic vasculitis; and (5) microbial sterility.
类风湿性嗜中性皮病(RND)与类风湿性关节炎相关,通常表现为双侧肢体上的丘疹、结节和/或斑块。罕见情况下,可出现水疱大疱性皮损(大疱性RND)。我们在此报告1例在我科诊断的大疱性RND病例。一名70岁日本女性,下肢出现多个疼痛性紧张大疱,伴有脓疱、红斑丘疹和糜烂,足底可见少数出血性大疱。她有14年血清阳性类风湿性关节炎病史,曾口服泼尼松龙和水合他克莫司成功治疗,但在就诊前1个月出现关节疼痛和肿胀。小腿水疱的皮肤活检显示表皮内和表皮下水疱,含有大量中性粒细胞。真皮中可见明显的嗜中性粒细胞浸润,有显著的核尘,但无血管炎。直接免疫荧光检查结果为阴性。水疱的细菌培养无菌。综合判断,诊断为大疱性RND。尽管口服米诺环素治疗1周,但仍有新的皮肤损害出现。治疗改为每日75mg氨苯砜,1周内皮肤损害和关节痛有所改善。在本报告中,我们描述了1例大疱性RND病例,并比较了大疱性和非大疱性RND临床表现的差异,此前尚无相关文献报道。此外,由于RND和Sweet综合征有重叠的临床病理特征,我们提出了RND的五条诊断标准:(1)确诊类风湿性关节炎;(2)类风湿性关节炎疾病活动度高;(3)多个红斑丘疹、结节、斑块和/或紧张性水疱大疱性皮损;(4)主要为嗜中性粒细胞真皮浸润,无白细胞破碎性血管炎;(5)微生物培养无菌。