Lin Xiaofeng, Zhang Wei, Zhou Ping
Department of Neonatology, Shenzhen Baoan Women's and Children's Hospital, Shenzhen, China.
Department of Research and Development, BGI Genomics, Shenzhen, China.
Front Pediatr. 2024 May 21;12:1338054. doi: 10.3389/fped.2024.1338054. eCollection 2024.
This article reports a case of neonatal incontinentia pigmenti onset in only one male monozygotic twin with characteristic skin lesions after birth followed by severe cerebrovascular lesions.
A male infant, the first of monozygotic twins, was born with multiple yellow pustules all over his body, repeated new herpes at different sites during the course of the disease, aggravated by fusion, warty crusts, and hyperpigmentation; biopsy pathology suggested eosinophilic spongiform edema of the skin. Peripheral blood eosinophils were significantly elevated, and brain magnetic resonance imaging revealed diffuse multiple cystic and lamellar abnormal signal areas in the left frontal and parietal lobes. On day 30, the infant showed neurological symptoms, such as poor response and apnea, and an emergency cranial computed tomography scan revealed abnormal changes in the left cerebral hemisphere and bilateral cerebellum. After admission, he was given a potassium permanganate bath and topical mupirocin for 1 month, and the skin abnormalities improved. He was treated with mechanical ventilation and vasoactive drugs for 2 days after the cerebrovascular accident, and died the same day after the parents chose hospice care. No deletion variants or point mutations were detected in subsequent genetic tests, and chromosomal copy number variation tests revealed different degrees of chimeric duplications and deletions in different regions of chromosomes Y and 3. The parents were healthy, and his twin brother had normal growth and development with no abnormalities at multiple follow-up visits.
Neonatal incontinentia pigmenti in only one male monozygotic twin is extremely rare and the genetic diagnosis is challenging. Awareness of the combined cerebrovascular lesions needs to be enhanced, and potential prevention and treatment methods need to be explored to improve the prognosis.
本文报道了一例仅在单卵双胎中的一名男性新生儿发生色素失禁症的病例,该患儿出生后即出现特征性皮肤损害,随后出现严重的脑血管病变。
一名男性婴儿,为单卵双胎中的老大,出生时全身布满多个黄色脓疱,病程中不同部位反复出现新发疱疹,融合后加重,形成疣状结痂及色素沉着;活检病理提示皮肤嗜酸性海绵状水肿。外周血嗜酸性粒细胞显著升高,脑部磁共振成像显示左侧额叶和顶叶弥漫性多发囊性及层状异常信号区。出生后30天,患儿出现反应差、呼吸暂停等神经症状,急诊头颅计算机断层扫描显示左侧大脑半球及双侧小脑异常改变。入院后给予高锰酸钾浴及外用莫匹罗星治疗1个月,皮肤异常改善。脑血管意外发生后给予机械通气及血管活性药物治疗2天,在父母选择临终关怀后于当日死亡。后续基因检测未检测到缺失变异或点突变,染色体拷贝数变异检测显示Y染色体和3号染色体不同区域存在不同程度的嵌合重复和缺失。父母身体健康,其双胞胎弟弟生长发育正常,多次随访均无异常。
仅在单卵双胎中的一名男性新生儿发生色素失禁症极为罕见,基因诊断具有挑战性。需要提高对合并脑血管病变的认识,并探索潜在的预防和治疗方法以改善预后。