Congenital hepatic fibrosis -: A very uncommon cause of pancytopenia in children

被引：2

作者：

Trizzino, A ^{[1
]}

Farruggia, P

Russo, D

D'Angelo, P

Tropia, S

Benigno, V

Tarantino, G

Di Marco, V

Aricò, M

机构：

[1] Osped Bambini G Di Cristina,Via Benedettini 1, I-90134 Palermo, Italy

[2] Osped San Giovanni Dio, UO Pediat, Agrigento, Italy

[3] Univ Palermo, Cattedra Gastroenterol, Palermo, Italy

来源：

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | 2005年 / 27卷 / 10期

关键词：

splenomegaly; cytopenia; polycystic kidney disease;

D O I：

10.1097/01.mph.0000184577.46458.7e

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

The disease presentation of autosomal recessive polycystic kidney disease (OMIM #263200, ARPKD) is highly variable and includes polycystic kidneys, pulmonary hypoplasia, and congenital hepatic fibrosis. The authors report an unusual case of ARPKD presenting with hepatosplenornegaly and cytopenia mimicking acute leukemia.

引用

页码：567 / 568

页数：2

共 18 条

[1] Phenotypic Variation and Long-Term Outcome in Children With Congenital Hepatic Fibrosis
Rawat, Dinesh
Kelly, Deirdre A.
Milford, David V.
Sharif, Khalid
Lloyd, Carla
McKiernan, Patrick J.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2013, 57 (02) : 161 - 166
[2] Liver transplantation for congenital hepatic fibrosis
Wu, Wei Kelly
Ziogas, Ioannis A.
Izzy, Manhal
Pai, Anita K.
Hafberg, Einar T.
Matsuoka, Lea K.
Alexopoulos, Sophoclis P.
TRANSPLANT INTERNATIONAL, 2021, 34 (07) : 1281 - 1292
[3] Congenital hepatic fibrosis (a case report)
Popovych, O. O.
Moroz, L., V
Avdosiev, Yu, V
Chabanov, F. A.
Voinalovych, O. O.
ZAPOROZHYE MEDICAL JOURNAL, 2021, 23 (06) : 882 - 888
[4] WHAT IS CONGENITAL HEPATIC-FIBROSIS
DESMET, VJ
HISTOPATHOLOGY, 1992, 20 (06) : 465 - 477
[5] Congenital Hepatic Fibrosis in Children and Adults: Clinical Manifestations, Management, and Outcome-Case Series and Literature Review
Zhu, Beidi
Du, Zunguo
Wang, Zhengxin
Li, Yang
Zhang, Jiming
Zhu, Haoxiang
GASTROENTEROLOGY RESEARCH AND PRACTICE, 2020, 2020
[6] CONGENITAL HEPATIC FIBROSIS WITHOUT ANY SYMPTOMS AS DIAGNOSED BY LAPAROSCOPY
Kisaka, Yoshiyasu
Abe, Masanori
Tokumoto, Yoshio
Hirooka, Masashi
Shigematsu, Shuichiro
Koizumi, Yohei
Murakami, Hidehiro
Matsuura, Bunzo
Hiasa, Yoichi
Onji, Morikazu
DIGESTIVE ENDOSCOPY, 2010, 22 (04) : 357 - 359
[7] Congenital hepatic fibrosis leading to cirrhosis and hepatocellular carcinoma: A case report
Ghadir M.R.
Bagheri M.
Ghanooni A.H.
Journal of Medical Case Reports, 5 (1)
[8] Macrophage Recruitment by Fibrocystin-Defective Biliary Epithelial Cells Promotes Portal Fibrosis in Congenital Hepatic Fibrosis
Locatelli, Luigi
Cadamuro, Massimiliano
Spirli, Carlo
Fiorotto, Romina
Lecchi, Silvia
Morell, Carola Maria
Popov, Yury
Scirpo, Roberto
De Matteis, Maria
Amenduni, Mariangela
Pietrobattista, Andrea
Torre, Giuliano
Schuppan, Detlef
Fabris, Luca
Strazzabosco, Mario
HEPATOLOGY, 2016, 63 (03) : 965 - 982
[9] Congenital Hepatic Fibrosis in a Case of Autosomal Dominant Polycystic Kidney Disease: A Case Report
Majethia, Nikhil
Haria, Pankti
Patel, R. D.
Gadgil, Nitin
Kalgutkar, Alka
INTERNATIONAL JOURNAL OF SCIENTIFIC STUDY, 2014, 2 (08) : 243 - 245
[10] Congenital hepatic fibrosis: clinical presentation, laboratory features and management at a tertiary care hospital of Lahore
Parkash, Arit
Cheema, Huma Arshad
Malik, Hassan Suleman
Fayyaz, Zafar
JOURNAL OF THE PAKISTAN MEDICAL ASSOCIATION, 2016, 66 (08) : 984 - 988

← 1 2 →