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维生素K缺乏的不寻常表现——结节性紫癜:病例系列

Unusual Manifestation of Vitamin K Deficiency, Nodular Purpura: A Case Series.

作者信息

Ballal Sumedha, Prathibha J P, Pinto Althea V, Srinivasa Sanjanaa, Augustine Mary

机构信息

Department of Dermatology, St John's Medical College, Bangalore, Karnataka, India.

Department of Dermatology, Kasturba Medical College, Mangalore, Karnataka, India.

出版信息

Indian Dermatol Online J. 2024 Dec 11;16(1):132-136. doi: 10.4103/idoj.idoj_557_24. eCollection 2025 Jan-Feb.

Abstract

Vitamin K deficiency is a common entity in infancy characterized by bleeding from various sites, intracranial bleeding being the most commonly reported feature. Nodular purpura is an uncommon manifestation of vitamin K deficiency in infancy with a few reported cases in literature. We present four cases of infants presenting with nodular purpura as a manifestation of late-onset vitamin K deficiency bleeding (VKDB). All four children presented with asymptomatic bluish-gray nodules, along with symptoms of hepatic dysfunction. Coagulation profile was deranged in all four children and symptoms improved with the administration of parenteral Vitamin K. The case series details the clinical course, treatment response, and follow-up for each patient. To conclude, nodular purpura can be a rare presentation of late-onset VKDB. "Warning bleeds" of VKDB are known to precede dangerous intracranial bleeds. Late-onset VKDB cannot be prevented by routine neonatal vitamin K prophylaxis and requires repeated vitamin K treatments. The case series is an attempt to highlight the unusual manifestation of a bleeding disorder that can be easily prevented by early intervention.

摘要

维生素K缺乏在婴儿期是一种常见情况,其特征为身体各部位出血,颅内出血是最常报告的特征。结节性紫癜是婴儿期维生素K缺乏的一种罕见表现,文献中仅有少数病例报道。我们报告了4例以结节性紫癜为迟发性维生素K缺乏出血(VKDB)表现的婴儿病例。所有4名儿童均出现无症状的蓝灰色结节,并伴有肝功能障碍症状。所有4名儿童的凝血指标均紊乱,经肠外补充维生素K后症状改善。该病例系列详细介绍了每位患者的临床病程、治疗反应及随访情况。总之,结节性紫癜可能是迟发性VKDB的一种罕见表现。已知VKDB的“警示性出血”先于危险的颅内出血。常规新生儿维生素K预防措施无法预防迟发性VKDB,需要重复进行维生素K治疗。该病例系列旨在突出一种出血性疾病的不寻常表现,通过早期干预可轻易预防。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33b8/11753556/78edcfa3b91a/IDOJ-16-132-g001.jpg

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