Congenital Prothrombin Deficiency: A Rare Cause of Puberty Menorrhagia

Swaramya Ch, rasekaran, H. Sagili, P. Dasari
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Abstract

During the transitioning through puberty, adolescents present with varied gynaecological issues, among which puberty menorrhagia is a significant complaint. The most common underlying cause of puberty menorrhagia is anovulation, other causes being endocrine dysfunction, PCOS and bleeding disorders. Congenital prothrombin deficiency is an extremely rare inherited coagulopathy, affecting one in two million of general population. Depending on the severity of deficiency they present with myriad bleeding tendencies, including epstaxis, soft tissue bleeds, GI hemorrhage, intracranial hemorrhage, menorrhagia, excessive post traumatic and post-surgical bleeding. Here, we present a very rare case of congenital prothrombin deficiency presenting primarily with puberty menorrhagia.
先天性凝血酶原缺乏:青春期月经过多的罕见原因
在青春期过渡期间,青少年出现各种妇科问题,其中青春期月经过多是一个重要的投诉。青春期月经过多最常见的潜在原因是无排卵,其他原因是内分泌功能障碍,多囊卵巢综合征和出血性疾病。先天性凝血酶原缺乏症是一种极其罕见的遗传性凝血疾病,一般人群发病率为百万分之一。根据缺乏的严重程度,他们表现出无数的出血倾向,包括脓血、软组织出血、胃肠道出血、颅内出血、月经过多、创伤后和术后出血。在这里,我们提出一个非常罕见的先天性凝血酶原缺乏,主要表现为青春期月经过多。
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