Moyamoya Disease in a Child With Fanconi Anemia: An Anomaly or a Complication

被引：0

作者：

Alavi, Samin ^{[1
]}

Khalili, Mitra ^{[2
]}

Khaffafpour, Zahra ^{[3
]}

Shams, Negar ^{[4
]}

机构：

[1] Shahid Beheshti Univ Med Sci, Res Inst Childrens Hlth, Pediat Congenital Hematol Disorders Res Ctr, Hematol Oncol, Tehran, Iran

[2] Shahid Beheshti Univ Med Sci, Mofid Childrens Hosp, Pediat Radiol, Tehran, Iran

[3] Shahid Beheshti Univ Med Sci, Res Inst Childrens Hlth, Pediat Congenital Hematol Disorders Res Ctr, Pediat Hematol Oncol, Tehran, Iran

[4] Shahid Beheshti Univ Med Sci, Res Inst Childrens Hlth, Pediat Congenital Hematol Disorders Res Ctr, Gen Practice, Tehran, Iran

来源：

CUREUS JOURNAL OF MEDICAL SCIENCE | 2024年 / 16卷 / 02期

关键词：

bilateral disease; mri; internal carotid artery; moyamoya disease; fanconi anemia;

D O I：

10.7759/cureus.54455

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Fanconi anemia (FA) is an inherited bone marrow failure syndrome associated with congenital anomalies and a predisposition to cancer. We report the case of a 9 -year -old boy with FA who developed an abrupt onset of hemiplegia and dysarthria. The diagnosis of moyamoya disease (MMD) was suggested by magnetic resonance angiography (MRA) which demonstrated severe stenosis in the right internal carotid artery along with collateral vessel formation in the right basal ganglia. It is questioned whether the moyamoya pattern in this case is part of congenital malformations associated with FA or is the result of recurrent bleedings around the carotid siphon.

引用

页数：8

共 14 条

[1] Central nervous system lesions in Fanconi anemia: Experience from a research center for Fanconi anemia patients [J].

Aksu, Tekin ;

Gumruk, Fatma ;

Bayhan, Turan ;

Coskun, Cagri ;

Oguz, Kader K. ;

Unal, Sule .

PEDIATRIC BLOOD & CANCER, 2020, 67 (12)

[2] Fanconi anemia associated with moyamoya disease in Saudi Arabia [J].

Al-Hawsawi, Zakaria M. ;

Al-Zaid, Mohamed A. ;

Barnawi, Ashwaq I. ;

Yassine, Saadeddine M. .

SAUDI MEDICAL JOURNAL, 2015, 36 (02) :233-235

[3] Fanconi anemia and its diagnosis [J].

Auerbach, Arleen D. .

MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2009, 668 (1-2) :4-10

[4]

COHEN N, 1980, PEDIATRICS, V65, P804

[5] SPECTRUM OF ANOMALIES IN FANCONI ANEMIA [J].

GLANZ, A ;

FRASER, FC .

JOURNAL OF MEDICAL GENETICS, 1982, 19 (06) :412-416

[6] Adult Moyamoya Disease and Syndrome: Current Perspectives and Future Directions: A Scientific Statement From the American Heart Association/American Stroke Association [J].

Gonzalez, Nestor R. ;

Amin-Hanjani, Sepideh ;

Bang, Oh Young ;

Coffey, Christopher ;

Du, Rose ;

Fierstra, Jorn ;

Fraser, Justin F. ;

Kuroda, Satoshi ;

Tietjen, Gretchen E. ;

Yaghi, Shadi .

STROKE, 2023, 54 (10) :E465-E479

[7] Moyamoya disease: diagnosis and interventions [J].

Ihara, Masafumi ;

Yamamoto, Yumi ;

Hattori, Yorito ;

Liu, Wanyang ;

Kobayashi, Hatasu ;

Ishiyama, Hiroyuki ;

Yoshimoto, Takeshi ;

Miyawaki, Satoru ;

Clausen, Tim ;

Bang, Oh Young ;

Steinberg, Gary K. ;

Tournier-Lasserve, Elisabeth ;

Koizumi, Akio .

LANCET NEUROLOGY, 2022, 21 (08) :747-758

[8] Corresponding author: Satoshi Kuroda, MD, PhD . e-mail: [J].

Kuroda, Satoshi ;

Fujimura, Miki ;

Takahashi, Jun ;

Kataoka, Hiroharu ;

Ogasawara, Kuniaki ;

Iwama, Toru ;

Tominaga, Teiji ;

Miyamoto, Susumu .

NEUROLOGIA MEDICO-CHIRURGICA, 2022, 62 (07) :307-312

[9]

Mahato M P, 2011, BMJ Case Rep, V2011, DOI 10.1136/bcr.01.2010.2680

[10] FANCONI-ANEMIA AND MOYAMOYA - EVIDENCE FOR AN ASSOCIATION [J].

PAVLAKIS, SG ;

VERLANDER, PC ;

GOULD, RJ ;

STRIMLING, BC ;

AUERBACH, AD .

NEUROLOGY, 1995, 45 (05) :998-1000

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