慢性肉芽肿病患者骨髓移植后出现坏死性溃疡性口炎1例。

IF 0.9 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
Lama Alabdulaaly, Christy Lucas, Susan Prockop, Birgitta Schmidt, Nathaniel Treister, Herve Sroussi
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引用次数: 0

摘要

背景:慢性肉芽肿病(CGD)是一种以危及生命的感染和炎症为特征的先天性免疫错误。同种异体造血干细胞移植(alloHSCT)具有潜在的治愈性。坏死性牙周病(npd)是罕见的,可以在免疫功能低下/免疫抑制的个体中看到,但在CGD患者中尚未报道。我们报告了一例CGD移植患者的坏死性口炎(NS)形式的NPD。方法:一名12岁男性,以严重的牙龈疼痛为表现。患者的病史对于4岁时诊断的x连锁CGD和杂合RIPK1突变具有重要意义。患者接受了来自不匹配的非亲属供体的同种异体造血干细胞移植。同种异体造血干细胞移植后第61天的口腔内检查显示多灶性牙龈溃疡,短期泼尼松和局部地塞米松口服溶液对溃疡无反应。溃疡进展到唇黏膜和软腭/扁桃体(第88天)。结果:软腭/扁桃体区活检显示深度急性炎症和脓肿,符合NS的诊断。患者于第103天行深度牙龈洗牙,并给予阿莫西林和甲硝唑治疗。患者在移植后第125天口腔溃疡完全消退,但在第314天出现慢性移植物抗宿主病,并累及口腔黏膜。结论:我们报告了首例异体造血干细胞移植的并发症,该患者接受了抗生素治疗、牙周清创和停用潜在触发药物。我们的报告表明,异位造血干细胞移植后可能发生NS/NPD。重点:慢性肉芽肿病是一种遗传性多系统自身炎症。慢性肉芽肿病患者可能有口腔表现,包括口腔溃疡和牙龈炎/牙周炎。坏死性溃疡性口炎可能在造血干细胞移植后出现。摘要:慢性肉芽肿病(CGD)是一种损害免疫系统的疾病,可以通过骨髓移植来治疗。坏死性牙周病(NPD)是一组影响口腔并导致组织死亡(坏死)的罕见疾病,临床上表现为口腔溃疡(口腔溃疡)。在这篇文章中,我们报告了一个接受骨髓移植治疗CGD的儿童的NPD。本报告拓宽了移植后口腔溃疡的鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Necrotizing ulcerative stomatitis following bone marrow transplantation in a patient with chronic granulomatous disease: Case report.

Background: Chronic granulomatous disease (CGD) is an inborn error of immunity characterized by life-threatening infections and inflammation. Allogeneic hematopoietic stem cell transplantation (alloHSCT) is potentially curative. Necrotizing periodontal diseases (NPDs) are rare and can be seen in immunocompromised/immunosuppressed individuals but have not been reported in patients with CGD. We report NPD in the form of necrotizing stomatitis (NS) in a patient transplanted for CGD.

Methods: A 12-year-old male presented with severe gingival pain. The patient's medical history was significant for X-linked CGD diagnosed at 4 years of age and a heterozygous RIPK1 mutation. The patient underwent alloHSCT from a mismatched unrelated donor. Intraoral examination on day +61 post-alloHSCT revealed multifocal gingival ulceration, which did not respond to a short course of prednisone and topical dexamethasone oral solution. The ulcers progressed to involve the lip mucosa and soft palate/tonsil (day +88).

Results: Biopsy from the soft palate/tonsillar area showed deep acute inflammation and abscesses consistent with the diagnosis of NS. The patient underwent deep gingival scaling on day +103 and received amoxicillin and metronidazole. The patient had complete resolution of the oral ulcers by day +125 but developed chronic graft-versus-host disease involving the oral mucosa on day +314 post-alloHSCT.

Conclusion: We report the first case of NS as a complication of alloHSCT in a patient transplanted for CGD which was successfully managed with antibiotic therapy, periodontal debridement, and discontinuation of potentially triggering agents. Our report demonstrates that NS/NPD may occur in post-alloHSCT setting.

Key points: Chronic granulomatous disease is an inherited multisystem autoinflammatory condition. Patients with chronic granulomatous disease may have oral manifestations including oral ulcerations and gingivitis/periodontitis. Necrotizing ulcerative stomatitis may arise in the post-hematopoietic stem cell transplantation setting.

Plain language summary: Chronic granulomatous disease (CGD) is a condition that impairs the immune system and can be managed with bone marrow transplantation. Necrotizing periodontal disease (NPD) are a group of rare conditions that affect the mouth and cause tissue death (necrosis) and present clinically as oral ulcers (mouth sores). In this article, we report NPD in a child who received bone marrow transplantation for his CGD. This report broadens the differential diagnosis of oral ulcers in the post-transplant setting.

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Clinical Advances in Periodontics
Clinical Advances in Periodontics DENTISTRY, ORAL SURGERY & MEDICINE-
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