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A Rare Case Of Endometrial Ossification

机译:罕见的子宫内膜骨化症

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We report a rare case of endometrial ossification in a 28 year old female, who presented with abdominal pain, menorrhagia and secondary infertility. On transvaginal ultrasonography, a hyper-echoic area within the uterine cavity, suggestive of an intra-uterine foreign body was noted. Histopathological examination of the endometrial curettage showed bony spicules with inflammatory cells infiltration. There was no evidence of malignancy. Introduction Endometrial osseous metaplasia, an uncommon entity which is related to secondary infertility following an abortion, is the presence of mature and immature bone in the endometrium. Less than 100 cases have been reported in the world literature, including nine from India [1],[2],[3].. Most of the patients conceive after the hysteroscopic evacuation of the bony spicules [4],[5]. We are reporting a case of endometrial ossification in a 28 year old female, who presented with menorrhagia and secondary infertility. Case Summary A 28 year old female patient presented to Gynecological Out Patient Department with the complaints of abdominal pain, menorrhagia and secondary infertility. Her past history revealed that she had one living child and two repeated abortions 6 years back, after which she had failed to conceive. Dilatation and curettage was done at 4 months of gestation during the last conception. The patient had no known history of systemic disease. The patient had no signs or laboratory findings which suggested a calcium metabolism disorder. Her serum calcium and phosphorus levels were normal. Further evaluation by ultrasonography revealed a densely echogenic band occupying most of the endometrial cavity. The patient underwent diagnostic hysteroscopy which revealed a single firm to hard tissue piece within the endometrial cavity, which were removed by using hysteroscopic forceps and these were submitted for histopathological study.Grossly, the biopsy specimen included multiple, small, firm to hard tissue bits, along with scanty soft tissue pieces, together measuring 1×0.5×0.5 cms in dimension.(figure 1) The hard tissue bits were kept for decalcification. The hematoxylin and eosin stained paraffin sections were subjected for microscopic examination. The sections showed fragmented endometrial tissue which was predominantly composed of tubular glands with scanty stroma. The osteoid tissue which was mainly composed of the trabeculae of woven bone was present surrounding the endometrial tissue and inflammatory cells. The endometrial glands did not show any secretory activity. Further examination did not reveal any granuloma, necrosis or the products of conception. The histological diagnosis of osseous metaplasia of the endometrium was made.(figure 2)
机译:我们报道了一名28岁女性的子宫内膜骨化罕见病例,该女性表现为腹痛,月经过多和继发性不孕。经阴道超声检查发现子宫腔内有高回声区,提示子宫内异物。子宫内膜刮除术的组织病理学检查显示,骨性针头有炎性细胞浸润。没有证据表明有恶性肿瘤。引言子宫内膜骨化生是一种不常见的实体,与流产后的继发性不孕有关,是子宫内膜中存在成熟而未成熟的骨。世界文献报道少于100例,其中9例来自印度[1],[2],[3]。大多数患者在宫腔镜抽空骨针后受孕[4],[5]。我们正在报告一名28岁女性的子宫内膜骨化病例,该女性患有月经过多和继发性不孕。病例摘要一名28岁的女性患者因腹部疼痛,月经过多和继发性不孕症而到妇科门诊就诊。她的过去历史表明,六年前,她有一个活着的孩子,两次流产,此后她一直没有怀孕。在最后一次受孕期间,在妊娠4个月时进行了刮宫术。该患者没有全身性疾病的病史。患者没有迹象或实验室检查结果提示钙代谢异常。她的血清钙和磷水平正常。通过超声检查的进一步评估显示出密集的回声带占据了子宫内膜腔的大部分。该患者接受了诊断性宫腔镜检查,发现子宫内膜腔内有一个坚固的硬组织块,并使用宫腔镜钳将其切除,并提交组织病理学研究。总的来说,活检标本包括多个小而坚固的硬组织碎片,连同稀薄的软组织碎片一起,尺寸为1×0.5×0.5 cms。(图1)保留硬组织碎片用于脱钙。对苏木精和曙红染色的石蜡切片进行显微镜检查。切片显示子宫内膜组织破碎,主要由具有少量基质的小管腺组成。存在于子宫内膜组织和炎性细胞周围的类骨组织主要由编织骨的小梁组成。子宫内膜腺未显示任何分泌活性。进一步检查未发现肉芽肿,坏死或受孕产物。进行了子宫内膜骨化生的组织学诊断。(图2)

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