multicystic

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  • 文章类型: Case Reports
    一个身材矮小、智商低的19岁女孩,难以辨认的演讲,在妇科门诊部看到腹部大大扩张。她接受了调查,发现有较大的腹肾盂多囊性卵巢,无恶性特征,绝经前妇女的CA125水平在正常范围内。她的促甲状腺激素(TSH)显着升高。她被诊断为未经治疗的严重甲状腺功能减退伴良性巨大卵巢囊肿,构成囊肿破裂和迫在眉睫的并发症的严重风险。父母得到了建议,他们接受了风险,同意保守治疗.左甲状腺素替代疗法开始,一个月后,她的TSH水平恢复正常.治疗一个月后的随访超声检查显示卵巢囊肿大小明显减小。继续进行甲状腺替代治疗,三个月后,囊肿消失了,和卵巢,小得多,卵巢形态多囊。仔细分析临床体征,调查,适当的治疗有助于避免不必要的手术。
    A 19-year-old girl with a short stature and presenting low intelligence quotient, illegible speech, and a greatly distended abdomen was seen at the gynecological outpatient department. She underwent investigation and was found to have large abdominopelvic multicystic ovaries with no malignant features and CA125 levels within the normal range for premenopausal women. Her thyroid-stimulating hormone (TSH) was markedly elevated. She received a diagnosis of untreated severe hypothyroidism with benign giant ovarian cysts, posing a grave risk of cyst rupture and imminent complications. The parents were counseled, and they accepted the risk, agreeing to conservative therapy. Levothyroxine replacement therapy was initiated, and after one month, her TSH levels normalized. Follow-up ultrasonography after one month of her therapy revealed a marked decrease in ovarian cyst size. Thyroid replacement therapy was continued, and at the end of three months, the cysts disappeared, and the ovaries, much smaller, showed polycystic ovarian morphology. Careful analysis of clinical signs, investigations, and appropriate therapy helped avoid unnecessary surgery.
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  • 文章类型: Review
    孤立性纤维瘤(SFT)是一种罕见的间充质肿瘤,已知发生在各种软组织和内脏位置。肾脏是这些肿瘤的罕见部位之一,文献中约有64例。大多数肾脏SFT是棕白色的,固体,公司,未封装,和分叶肿块。在文献中从未报道过主要是囊性肾SFT。在此,我们描述了一名44岁男性的多囊性肾SFT病例,该病例具有特征性CD34/STAT6免疫表型。在处理肾脏和SFT的囊性梭形细胞肿瘤时,必须进行仔细的总体和显微镜检查,在鉴别诊断中应始终考虑SFT。STAT6免疫组织化学对于诊断相当特异。莫雷索,由于具有重要的治疗和预后意义,因此需要详细的免疫分析来排除其他肾脏梭形细胞肿瘤。
    Solitary fibrous tumor (SFT) is a rare mesenchymal neoplasm known to occur at various soft tissue and visceral locations. Kidney is one of the rare locations for these tumors with around 64 cases being available in the literature. Most of the renal SFTs are tan-white, solid, firm, unencapsulated, and lobulated masses. A predominantly cystic renal SFT has never been reported in the literature. Herein we describe a case of multicystic renal SFT in a 44-year-old male with the characteristic CD34 + /STAT6 + immunophenotype. A careful gross and microscopic examination is warranted while dealing with cystic spindle cell neoplasms of the kidney and SFT should always be considered in the differential diagnosis. STAT6 immunohistochemistry is quite specific for the diagnosis. Moreso, a detailed immunopanel is necessary to exclude other spindle cell neoplasms of the kidney because of significant therapeutic and prognostic implications.
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