Department of Gastroenterology, Fukushima Rosai Hospital, Uchigo, Iwaki, Fukushima, 973-8403, Japan.
Department of Gastroenterology, Fukushima Medical University School of Medicine, Fukushima, Japan.
BMC Gastroenterol. 2021 Dec 20;21(1):488. doi: 10.1186/s12876-021-02065-0.
Gastrointestinal lesions, which sometimes develop in Behçet's disease (BD), are referred to as intestinal BD. Although rare, intestinal BD can be accompanied by myelodysplastic syndrome (MDS) with abnormal karyotype trisomy 8, which is refractory to immunosuppressive therapy. Pulmonary alveolar proteinosis is a rare lung complication of BD and MDS. Herein, we present an extremely rare case of intestinal BD presenting with MDS and several chromosomal abnormalities, followed by secondary pulmonary proteinosis.
A 58-year-old Japanese woman with a 3-year history of genital ulcers and oral aphthae was admitted to our hospital. The patient developed abdominal pain and persistent diarrhea. Colonoscopy revealed multiple, round, punched-out ulcers from the terminal ileum to the descending colon. Intestinal BD was diagnosed and the patient was treated with colchicine, prednisolone, and adalimumab. However, her symptoms were unstable. Bone marrow examination to investigate the persistent macrocytic anemia revealed the presence of trisomy 8, trisomy 9, and X chromosome abnormalities (48, + 8, + 9, X, i(X) (q10) in 12 out of the examined 20 cells). Based on her hypoplastic bone marrow, the patient was diagnosed with low-risk MDS (refractory anemia). At the age of 61, the patient developed pneumonia with fever and diffuse ground-glass opacities on the lung computed tomography (CT). Chest high-resolution CT and histopathology via transbronchial lung biopsy revealed the presence of pulmonary alveolar proteinosis (PAP). These findings combined with the underlying disease led to the diagnosis of secondary PAP.
Secondary pulmonary proteinosis may accompany intestinal BD with MDS and several chromosomal abnormalities. Physicians should pay attention to lung complications, such as PAP, in patients with intestinal BD complicated by MDS. Genetic abnormalities may be associated with the development of such diseases.
胃肠道病变,有时在贝赫切特病(BD)中发展,被称为肠 BD。尽管罕见,但肠 BD 可能伴有骨髓增生异常综合征(MDS)伴异常核型三体 8,对免疫抑制治疗有抗性。肺泡蛋白沉积症是 BD 和 MDS 的罕见肺部并发症。在此,我们报告了一例极其罕见的肠 BD 伴 MDS 和多种染色体异常,继而继发肺蛋白沉积症的病例。
一名 58 岁日本女性,生殖器溃疡和口腔阿弗他病史 3 年,因腹痛和持续性腹泻入院。结肠镜检查显示从末端回肠到降结肠有多个圆形、穿孔性溃疡。诊断为肠 BD,给予秋水仙碱、泼尼松龙和阿达木单抗治疗。然而,她的症状不稳定。为了研究持续性巨细胞性贫血,对骨髓进行了检查,结果显示存在三体 8、三体 9 和 X 染色体异常(在 20 个检查细胞中的 12 个中存在 48、+8、+9、X、i(X)(q10))。根据其骨髓增生不良,患者被诊断为低危 MDS(难治性贫血)。61 岁时,患者因发热和肺部 CT 弥漫性磨玻璃影而发生肺炎。经支气管镜肺活检的胸部高分辨率 CT 和组织病理学检查显示存在肺泡蛋白沉积症(PAP)。这些发现结合基础疾病导致了继发性 PAP 的诊断。
继发性肺蛋白沉积症可能伴随肠 BD 伴 MDS 和多种染色体异常。医生应注意肠 BD 合并 MDS 患者的肺部并发症,如 PAP。遗传异常可能与这些疾病的发生有关。