Congenital mesoblastic nephroma: Its diverse clinical features – A literature review with a case report

2015 ◽  
Vol 36 (3) ◽  
pp. 340-344
Author(s):  
H. Takahashi ◽  
A. Ohkuchi ◽  
T. Kuwata ◽  
R. Usui ◽  
S. Takahashi ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Clinical Features ◽  
Mesoblastic Nephroma ◽  
Congenital Mesoblastic Nephroma

scholarly journals Cellular congenital mesoblastic nephroma detected by prenatal MRI: a case report and literature review

2021 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
Tingting Liu ◽  
Lika’a Fasih Y. Al-Kzayer ◽  
Shamil Naji Sarsam ◽  
Lei Chen ◽  
Raghad M. Saeed ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Mesoblastic Nephroma ◽  
Prenatal Mri ◽  
Congenital Mesoblastic Nephroma

Congenital mesoblastic nephroma rich from mitosis after in vitro fertilization: a case report

2008 ◽  
Vol 43 (5) ◽  
pp. e27-e29 ◽  
Author(s):  
Murat Yiğiter ◽  
İrfan Serdar Arda ◽  
Halil Kiyici ◽  
Akgün Hiçsönmez
Keyword(s):  
Case Report ◽  
In Vitro Fertilization ◽  
Mesoblastic Nephroma ◽  
Vitro Fertilization ◽  
Congenital Mesoblastic Nephroma

Congenital mesoblastic nephroma in a premature neonate - a case report

Pathology ◽  
2014 ◽  
Vol 46 ◽  
pp. S125
Author(s):  
Vincent Ikenna Onyekwelu ◽  
Charles Chidozie Anunobi ◽  
Kabir Bolarinwa Badmos ◽  
Nzechukwu Zimudo Ikeri
Keyword(s):  
Case Report ◽  
Premature Neonate ◽  
Mesoblastic Nephroma ◽  
Congenital Mesoblastic Nephroma

scholarly journals P02.55: Monochorionic diamniotic twins discordant for congenital mesoblastic nephroma: a case report

2006 ◽  
Vol 28 (4) ◽  
pp. 536-536
Author(s):  
E. Antolín ◽  
R. Pérez ◽  
J. León ◽  
O. Martínez ◽  
L. Ortiz
Keyword(s):  
Case Report ◽  
Mesoblastic Nephroma ◽  
Congenital Mesoblastic Nephroma

scholarly journals KONJENİTAL MEZOBLASTİK NEFROMA : OLGU SUNUMU [Congenital Mesoblastic Nephroma: Case Report]

2014 ◽  
Vol 45 (1) ◽  
pp. 22
Author(s):  
Mesut POLAT ◽  
Resul ARISOY ◽  
Emre ERDOĞDU ◽  
A.Doğukan ANGIN ◽  
Ahmet Semih TUĞRUL
Keyword(s):  
Case Report ◽  
Mesoblastic Nephroma ◽  
Congenital Mesoblastic Nephroma

scholarly journals UBA1 and DNMT3A Mutations in VEXAS Syndrome. A Case Report and Literature Review

2021 ◽  
Author(s):  
Farah Shaukat ◽  
Melissa Hart ◽  
Timothy Burns ◽  
Pankaj Bansal
Keyword(s):  
Bone Marrow ◽  
Case Report ◽  
Literature Review ◽  
Gene Mutation ◽  
Clinical Features ◽  
Somatic Mutation ◽  
Review Of Literature ◽  
Unique Case ◽  
Hematological Abnormalities ◽  
Autoinflammatory Condition

Abstract VEXAS syndrome is a recently described X-linked autoinflammatory condition associated with somatic mutation of the UBA1 gene. It often coexists with MDS which can occur due to DNMT3A mutation. These patients, predominantly males, present after the fifth decade of life with unique systemic inflammatory clinical features and have hematological abnormalities and vacuolated precursor cells on bone marrow pathology. Here we describe a unique case of VEXAS syndrome in a patient harboring DNMT3A gene mutation with coexisting UBA1 mutation with a review of literature.

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