一例罕见的III型胸膜肺母细胞瘤的免疫组织化学研究。

IF 0.8 4区 医学 Q4 PATHOLOGY
Siddhi Gaurish Sinai Khandeparkar, Maithili Mandar Kulkarni, Bageshri P Gogate, Chinmayee Sanjeev Dhavan
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引用次数: 0

摘要

在这里,我们打算用免疫组织化学(IHC)研究记录一例罕见的PPB III型病例,该病例发生在一名2岁男性中,其右半胸有广泛的肿瘤。胸膜肺母细胞瘤(PPB)是一种罕见的侵袭性、牙源性、儿童原发性胸内恶性肿瘤,高达25%的病例可发生在肺外,并附着在顶叶胸膜上。它在5岁以下的儿科人群中发现。它最初是由Manivel等人于1988年提出的一个独特的实体。PPB是原始间充质细胞的增殖,最初形成充满空气的囊肿,内衬良性上皮(I型,囊性)。后来,间充质细胞从囊肿中生长出来,形成局灶性实体区域(II型,实体和囊性),最后主要是实体块(III型,实体PPB)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of Pleuropulmonary blastoma type III with Immunohistochemical Study.

Here we intend to document a rare case of PPB type III in a 2-year male presenting with an extensive tumor occupying the right hemithorax with immunohistochemical (IHC) study. Pleuropulmonary blastoma (PPB) is a rare variably aggressive, dysodontogenetic, childhood primary intrathoracic malignancy which in up to 25% of cases can be extrapulmonary with attachment to the parietal pleura. It is found in pediatric population under 5 years of age. It was initially proposed as a distinct entity by Manivel et al. in 1988. PPB is a proliferation of primitive mesenchymal cells that initially form air-filled cysts lined by benign-appearing epithelium (type I, cystic). Later on, the mesenchymal cells outgrow the cysts with formation of focal solid areas (type II, solid and cystic) and finally, mainly solid mass (type III, solid PPB).

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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
422
审稿时长
1 months
期刊介绍: The journal will cover studies related to pathology including morbid anatomy, surgical pathology, clinical pathology, diagnostic cytopathology including gynecologic cytology and aspiration cytology, hematology including immuno-hematology and medical microbiology. The journal gives preference to clinically oriented studies over experimental and animal studies. The Journal would publish peer-reviewed original research papers, case reports, systematic reviews, meta-analysis, letters to the editor and brief communications. Review articles on current topics usually are invited by the editor.
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