Clinicopathological characteristics of placental chorioangioma: A clinicopathological study of 30 cases

Objective: The objective is to explore clinicopathological characteristics, diagnosis, differential diagnoses, treatment, and prognoses of placental chorioangioma (PCA). Materials and Methods: The pathological data of 30 cases of PCA were collected; the color Doppler ultrasound, Down’s screening, fe...

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Main Authors: Yuanyin Zheng, Xiaobin Liu, Yingyu Mao, Maohua Lin
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-12-01
Series:Indian Journal of Pathology and Microbiology
Subjects:
Online Access:https://journals.lww.com/10.4103/ijpm.ijpm_266_23
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author Yuanyin Zheng
Xiaobin Liu
Yingyu Mao
Maohua Lin
author_facet Yuanyin Zheng
Xiaobin Liu
Yingyu Mao
Maohua Lin
author_sort Yuanyin Zheng
collection DOAJ
description Objective: The objective is to explore clinicopathological characteristics, diagnosis, differential diagnoses, treatment, and prognoses of placental chorioangioma (PCA). Materials and Methods: The pathological data of 30 cases of PCA were collected; the color Doppler ultrasound, Down’s screening, fetal survival, and pathological characteristics were observed; and the literature was reviewed. Results: Of the 30 patients, the ages ranged from 20 to 38 years, with an average of 29.6 years. Pregnancy comorbidity occurred in 14 patients; intrauterine fetal death occurred in 4; the gross appearance of the tumor: a reddish-brown nodule, slightly round, 0.5–8 cm in diameter, can be seen on the cut surface of the placenta Pregnancy comorbidity occurred in 14 patients and intrauterine fetal death in 4. On sectioning the placenta, tumors grossly appeared as reddish-brown nodules, slightly round and ranging in diameter from 0.5 to 8 cm. Microscopically, the tumor has small, densely packed capillaries with fibrous connective tissue in the stroma. There were 10 cases with high risk of Down’s syndrome screening, and the immunophenotype CD34 (+) and Ki-67 proliferation index were less than 10%. Conclusions: PCA is rare and may be misdiagnosed as malignant tumor, which may be related to pregnancy comorbidity and high risk of Down’s screening, so improving the understanding of PCA can provide the basis for clinical diagnosis and intervention. PCA is a rare tumor which may be misdiagnosed as a malignancy. It may be related to pregnancy comorbidity and high risk of Down’s screening. Improving the understanding of PCA could provide the basis for clinical diagnosis and intervention.
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spelling doaj-art-03ec3f6b8a1f49cea208d9bbbfdce1eb2025-01-10T10:23:18ZengWolters Kluwer Medknow PublicationsIndian Journal of Pathology and Microbiology0377-49290974-51302024-12-0167477077410.4103/ijpm.ijpm_266_23Clinicopathological characteristics of placental chorioangioma: A clinicopathological study of 30 casesYuanyin ZhengXiaobin LiuYingyu MaoMaohua LinObjective: The objective is to explore clinicopathological characteristics, diagnosis, differential diagnoses, treatment, and prognoses of placental chorioangioma (PCA). Materials and Methods: The pathological data of 30 cases of PCA were collected; the color Doppler ultrasound, Down’s screening, fetal survival, and pathological characteristics were observed; and the literature was reviewed. Results: Of the 30 patients, the ages ranged from 20 to 38 years, with an average of 29.6 years. Pregnancy comorbidity occurred in 14 patients; intrauterine fetal death occurred in 4; the gross appearance of the tumor: a reddish-brown nodule, slightly round, 0.5–8 cm in diameter, can be seen on the cut surface of the placenta Pregnancy comorbidity occurred in 14 patients and intrauterine fetal death in 4. On sectioning the placenta, tumors grossly appeared as reddish-brown nodules, slightly round and ranging in diameter from 0.5 to 8 cm. Microscopically, the tumor has small, densely packed capillaries with fibrous connective tissue in the stroma. There were 10 cases with high risk of Down’s syndrome screening, and the immunophenotype CD34 (+) and Ki-67 proliferation index were less than 10%. Conclusions: PCA is rare and may be misdiagnosed as malignant tumor, which may be related to pregnancy comorbidity and high risk of Down’s screening, so improving the understanding of PCA can provide the basis for clinical diagnosis and intervention. PCA is a rare tumor which may be misdiagnosed as a malignancy. It may be related to pregnancy comorbidity and high risk of Down’s screening. Improving the understanding of PCA could provide the basis for clinical diagnosis and intervention.https://journals.lww.com/10.4103/ijpm.ijpm_266_23clinicopathological featureimmunohistochemistryplacental chorioangiomapregnancy comorbidities
spellingShingle Yuanyin Zheng
Xiaobin Liu
Yingyu Mao
Maohua Lin
Clinicopathological characteristics of placental chorioangioma: A clinicopathological study of 30 cases
Indian Journal of Pathology and Microbiology
clinicopathological feature
immunohistochemistry
placental chorioangioma
pregnancy comorbidities
title Clinicopathological characteristics of placental chorioangioma: A clinicopathological study of 30 cases
title_full Clinicopathological characteristics of placental chorioangioma: A clinicopathological study of 30 cases
title_fullStr Clinicopathological characteristics of placental chorioangioma: A clinicopathological study of 30 cases
title_full_unstemmed Clinicopathological characteristics of placental chorioangioma: A clinicopathological study of 30 cases
title_short Clinicopathological characteristics of placental chorioangioma: A clinicopathological study of 30 cases
title_sort clinicopathological characteristics of placental chorioangioma a clinicopathological study of 30 cases
topic clinicopathological feature
immunohistochemistry
placental chorioangioma
pregnancy comorbidities
url https://journals.lww.com/10.4103/ijpm.ijpm_266_23
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AT xiaobinliu clinicopathologicalcharacteristicsofplacentalchorioangiomaaclinicopathologicalstudyof30cases
AT yingyumao clinicopathologicalcharacteristicsofplacentalchorioangiomaaclinicopathologicalstudyof30cases
AT maohualin clinicopathologicalcharacteristicsofplacentalchorioangiomaaclinicopathologicalstudyof30cases