首页> 外文期刊>Human Pathology >Intravenous leiomyomatosis of the uterus: a clinicopathologic study of 18 cases, with emphasis on early diagnosis and appropriate treatment strategies.
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Intravenous leiomyomatosis of the uterus: a clinicopathologic study of 18 cases, with emphasis on early diagnosis and appropriate treatment strategies.

机译:子宫静脉平滑肌瘤病:18例临床病理研究,重点在于早期诊断和适当的治疗策略。

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Intravenous leiomyomatosis is a rare variant of leiomyoma that could result in death. Early and accurate diagnosis and appropriate treatment strategies play a dominant role in good prognosis. Eighteen cases of Intravenous leiomyomatosis , along with clinicopathologic data, were retrieved from our database. Most of the patients who ranged in age from 33 to 54 years (median, 44 years) presented with a pelvic mass or abnormal uterine bleeding. The diagnosis was confirmed by a immunohistochemical staining for smooth muscle actin, CD34, and Ki67. Surgical exploration confirmed the presence of a uterine mass (mean size, 5.08 cm). Wormlike plugs were identified within the broad ligament in 5 cases. The tumor penetrated to the inferior vena cava in 1 case. Histologic variants were noted in 33.33% (6/18) of our cases, which were classified as cellular intravenous leiomyomatosis (3 cases) and intravenous leiomyomatosis with papillary-like contour (1 case) and with fat metaplasia (2 cases). The 18 cases are made up 0.097% of all genital smooth muscle tumor cases of the hospital. The ratios of intravenous leiomyomatosis with uterine leiomyoma, with adenomyosis, with uterine leiomyoma and adenomyosis were 38.89% (7/18), 11.11% (2/18), and 27.78% (5/18), respectively. Follow-up information was available for 16 patients, with a follow-up duration of 26 to 104 months (mean, 55 months). Three cases (16.67%) recurred in patients younger than 40 years (33, 34, and 37 years). We propose that young patients undertake hysterectomy and unilateral salpingo-oophorectomy if they do not have any birthing requests. The cases of intravenous leiomyomatosis were underestimated because early diagnosis was easily missed. It is important to adequately sample all uterine leiomyomas and carefully examine the soft tissue on either side of the lower uterine segment below the peritoneal reflection to identify early-stage intravenous leiomyomatosis.
机译:静脉平滑肌瘤病是平滑肌瘤的一种罕见变异,可能导致死亡。早期准确的诊断和适当的治疗策略在良好的预后中起主导作用。从我们的数据库中检索出18例静脉平滑肌瘤病及其临床病理数据。年龄在33至54岁(中位数为44岁)的大多数患者出现盆腔肿块或异常子宫出血。通过平滑肌肌动蛋白,CD34和Ki67的免疫组织化学染色证实了诊断。手术探查证实存在子宫肿块(平均大小为5.08厘米)。 5例在宽韧带内发现蠕虫状栓塞。 1例肿瘤穿透下腔静脉。本组病例中有33.33%(6/18)发生组织学变异,分为细胞性静脉平滑肌瘤(3例)和具有乳头状轮廓和脂肪化生(2例)的静脉平滑肌瘤。这18例病例占医院所有生殖器平滑肌肿瘤病例的0.097%。静脉平滑肌瘤合并子宫平滑肌瘤,子宫腺肌病,子宫平滑肌瘤和子宫腺肌病的比例分别为38.89%(7/18),11.11%(2/18)和27.78%(5/18)。可获得16位患者的随访信息,随访时间为26到104个月(平均55个月)。 40岁以下(33、34和37岁)的患者中有3例(16.67%)复发。我们建议年轻患者如果没有生育要求,则要进行子宫切除术和单侧输卵管卵巢切除术。静脉平滑肌瘤病的病例被低估了,因为很容易错过早期诊断。重要的是要对所有子宫平滑肌瘤进行充分采样,并仔细检查子宫下腹段下方腹膜反射下方的软组织,以识别早期静脉平滑肌瘤病。

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