Cargando…

Co-existence of well-differentiated fetal adenocarcinoma of the lung with tuberculosis in a young female: A rare case report

RATIONALE: Fetal adenocarcinoma of the lung (FLAC) with fetal lung-like morphology is a rare entity of pulmonary adenocarcinoma. Well-differentiated fetal adenocarcinoma (WDFA) belongs to its the low-grade form, which possesses a relatively favorable prognosis. Tuberculosis (TB) is an aggressive inf...

Descripción completa

Detalles Bibliográficos
Autores principales:	Guo, Fengzhu, Wang, Jiantao, Hu, Haoyue, Xie, Xiaoxiao, Liu, Kuncheng, Luo, Feng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2019
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6919474/ https://www.ncbi.nlm.nih.gov/pubmed/31804370 http://dx.doi.org/10.1097/MD.0000000000018282

Ejemplares similares

Molecular diagnosis of sex chromosome mosaics in fetal amniotic cells
por: Fan, Zuqian, et al.
Publicado: (2021)

Antenatal screening and diagnosis of tuberous sclerosis complex by fetal echocardiography and targeted genomic sequencing
por: Gu, Xiaoyan, et al.
Publicado: (2018)

Fetal cardiac rhabdomyoma due to paternal mosaicism of TSC2: A case report
por: Chen, Lin, et al.
Publicado: (2020)

Whole exome sequencing combined with dynamic ultrasound assessments for fetal skeletal dysplasias: 4 case reports
por: Wang, Li, et al.
Publicado: (2022)

Retrospective analysis of genetic etiology and obstetric outcome of fetal cystic hygroma: A single-center study
por: Cai, Meiying, et al.
Publicado: (2022)

Association of Genetic Polymorphisms on VEGFA and VEGFR2 With Risk of Coronary Heart Disease
por: Liu, Doxing, et al.
Publicado: (2016)

Analysis of 17,428 pregnant women undergoing non-invasive prenatal testing for fetal chromosome in Northeast China
por: Dai, Rulin, et al.
Publicado: (2021)

Comprehensive analyses of potential key genes in active tuberculosis: A systematic review
por: Chen, Jiarui, et al.
Publicado: (2021)

The cGAS-STING pathway-related gene signature can predict patient prognosis and immunotherapy responses in prostate adenocarcinoma
por: Zhuo, Xingxing, et al.
Publicado: (2022)

Identification of THSD7B and PRMT9 mutations as risk factors for familial lung adenocarcinoma: A case report
por: Zhang, Qianqian, et al.
Publicado: (2023)

Fibrodysplasia ossificans progressiva in a young adult with genetic mutation: Case report
por: Wang, Zhankui, et al.
Publicado: (2021)

The genetic variants in calcium signaling related genes influence anti-tuberculosis drug induced liver injury: A prospective study
por: Lyu, Mengyuan, et al.
Publicado: (2019)

Clinical and genetic analysis of 2 rare cases of Wiskott–Aldrich syndrome from Chinese minorities: Two case reports
por: Liu, Haifeng, et al.
Publicado: (2021)

Wilson disease patient with rare heterozygous mutations in ATP7B accompanied by distinctive nocturnal enuresis: A case report
por: Zhang, Shijie, et al.
Publicado: (2020)

Identification of a rare missense mutation in GJB1 and prenatal diagnosis in a Chinese family with CMT: A case report
por: Huang, Xinyi, et al.
Publicado: (2022)

Association between the rs2106261 polymorphism in the zinc finger homeobox 3 gene and risk of atrial fibrillation: Evidence from a PRISMA-compliant meta-analysis
por: Wei, Yue, et al.
Publicado: (2021)

A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5: A pedigree-based case report
por: Tao, Tian, et al.
Publicado: (2020)

Aberrantly methylated-differentially expressed genes and related pathways in cholangiocarcinoma
por: Lin, Guan, et al.
Publicado: (2022)

Investigation of the IL-1β +3954 C>T polymorphism and the risk of sepsis: A case-control study
por: Fu, Peng, et al.
Publicado: (2020)

Profile of Differential Promoter Activity by Nucleotide Substitution at GWAS Signals For Multiple Sclerosis
por: Ryu, Jihye, et al.
Publicado: (2014)

Study on the differentially expressed genes and signaling pathways in dermatomyositis using integrated bioinformatics method
por: Liu, Wei, et al.
Publicado: (2020)

Association of the IL-13 polymorphisms rs1800925 and rs20541 with chronic obstructive pulmonary disease risk: An updated meta-analysis
por: Liao, Ning, et al.
Publicado: (2017)

Prenatal detection of pure proximal 6q14.1 microduplication encompassing LCA5 gene: A variant of likely benign
por: Yue, Fagui, et al.
Publicado: (2022)

Bioinformatic analysis of differentially expressed profiles of lncRNAs and miRNAs with their related ceRNA network in endometrial cancer
por: Li, Fengfan, et al.
Publicado: (2023)

Medical management of a child with congenital generalized lipodystrophy accompanied with progressive myoclonic epilepsy: A case report
por: Zhang, Yi, et al.
Publicado: (2019)

A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report
por: Xie, Dan, et al.
Publicado: (2023)

Constructing gene network for type 1 narcolepsy based on genome-wide association study and differential gene expression analysis (STROBE)
por: Ouyang, Hui, et al.
Publicado: (2020)

Identification of a cancer-associated fibroblast classifier for predicting prognosis and therapeutic response in lung squamous cell carcinoma
por: Lai, Xixi, et al.
Publicado: (2023)

HLA-A and HLA-B genes are involved in the pathogenesis of IBS
por: Liang, Huiping, et al.
Publicado: (2023)

Transthyretin-related hereditary amyloidosis with recurrent vomiting and renal insufficiency as the initial presentation: A case report
por: Xu, Jing, et al.
Publicado: (2017)

Correlation between SHBG gene polymorphism and male infertility in Han population of Henan province of China: A STROBE-compliant article
por: Cui, Yuan-rong, et al.
Publicado: (2017)

The relationship between VEGF-460(T>C) polymorphism and cancer risk: A systematic review and meta-analysis based on 46 reports
por: Qin, Haoran, et al.
Publicado: (2023)

Effects of individualized administration of folic acid on prothrombotic state and vascular endothelial function with H-type hypertension: A double-blinded, randomized clinical cohort study
por: Zhang, Song, et al.
Publicado: (2022)

Gene polymorphisms (rs324957, rs324981) in NPSR1 are associated with increased risk of primary insomnia: A cross-sectional study
por: Xie, Yuping, et al.
Publicado: (2020)

Genetic Variations in Key MicroRNAs are Associated With the Survival of Nonsmall Cell Lung Cancer
por: Wu, Shuangshuang, et al.
Publicado: (2015)

Performance characterization of PCR-free whole genome sequencing for clinical diagnosis
por: Zhou, Guiju, et al.
Publicado: (2022)

NOTCH3 Gene Polymorphism is Associated With the Prognosis of Gliomas in Chinese Patients
por: Shen, Zhipeng, et al.
Publicado: (2015)

Identification of X Monosomy Cells From a Gonad of Mixed Gonadal Dysgenesis With a 46,XY Karyotype: Case Report
por: Nishina-Uchida, Noriko, et al.
Publicado: (2015)

Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing
por: Wu, Chen-Chi, et al.
Publicado: (2015)

Functional Restriction for the Fear of Falling In Family Caregivers
por: Shen, Jing, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_soeg67in991n8iht12b2anbfmd