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卵巢类癌瘤:病例报告、系统文献回顾和汇总分析。

Ovarian Strumal Carcinoid: Case Report, Systematic Literature Review and Pooled Analysis.

机构信息

Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Medical Oncology, ASST Spedali Civili, Brescia, Italy.

1st Pathology Division, Department of Pathology and Laboratory Medicine, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Nazionale dei Tumori, Milan, Italy.

出版信息

Front Endocrinol (Lausanne). 2022 Apr 21;13:871210. doi: 10.3389/fendo.2022.871210. eCollection 2022.

Abstract

BACKGROUND

Ovarian strumal carcinoid is a rare tumor in which thyroid (struma) and carcinoid components coexist. The disease is generally considered to be a borderline malignancy, however, cases with metastatic disease have been described. No data in the literature are available to guide diagnosis and therapy.

METHODS

We performed a pooled analysis and a systematic review of histopathological-confirmed strumal carcinoid cases published in the literature using the following keywords: "strumal carcinoid of the ovary", "strumal carcinoid case report". A case of strumal carcinoid tumor diagnosed and followed-up at the Medical Oncology Unit of Spedali Civili (Brescia, Italy) was also described and included.

RESULTS

Sixty-six eligible publications were identified, providing data from one hundred and seventeen patients, plus a case diagnosed at our institution. At presentation, among the eighty-eight patients with symptomatic disease, 37% of patients suffered from abdominal distention and 49% from pain due to a growing abdominal tumor mass, 37% from constipation (peptide YY was analyzed in only nine of them, resulting above the physiologic range). Surgery was the primary therapy in 99% of the patients. Three patients had metastatic disease at diagnosis and five patients underwent recurrence after radical surgery. Histology at disease recurrence concerned the thyroid component in two patients, the carcinoid component in two patients, both histologies in one patient. Median disease-free survival and overall survival in this series were not attained.

CONCLUSION

Strumal carcinoid of the ovary generally presents a benign behavior and surgery is curative in most cases. However, a small group of patients with this disease can undergo disease recurrence due to both the thyroid and the neuroendocrine (carcinoid) components. A follow-up in radically operated patients is therefore needed, particularly in those with a voluminous disease at diagnosis.

摘要

背景

卵巢甲状腺类癌是一种罕见的肿瘤,其同时存在甲状腺(甲状腺肿)和类癌成分。该疾病通常被认为是一种交界性恶性肿瘤,但也有转移性疾病的病例描述。目前尚无文献数据可用于指导诊断和治疗。

方法

我们使用以下关键词对文献中已发表的经组织病理学证实的甲状腺类癌病例进行了汇总分析和系统评价:“卵巢甲状腺类癌”、“甲状腺类癌病例报告”。还描述并纳入了在意大利布雷西亚 Spedali Civili 医学肿瘤学病房诊断和随访的 1 例甲状腺类癌肿瘤病例。

结果

确定了 66 篇符合条件的出版物,提供了来自 117 名患者的数据,加上我们机构诊断的 1 例病例。在有症状的 88 例患者中,就诊时 37%的患者有腹胀,49%的患者因腹部肿瘤增大而疼痛,37%的患者有便秘(仅对其中 9 例分析了肽 YY,结果超过了生理范围)。99%的患者主要接受手术治疗。3 例患者在诊断时就有转移疾病,5 例患者在根治性手术后复发。2 例患者在疾病复发时出现甲状腺成分,2 例患者出现类癌成分,1 例患者出现两种组织学类型。本系列患者的中位无疾病生存和总生存均未达到。

结论

卵巢甲状腺类癌通常表现为良性行为,手术在大多数情况下可治愈。然而,一小部分患有这种疾病的患者可能会由于甲状腺和神经内分泌(类癌)成分而发生疾病复发。因此,需要对接受根治性手术的患者进行随访,特别是在诊断时疾病体积较大的患者。

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