Lymphomatoid granulomatosis in a patient with DOCK8 deficiency

被引：0
|
作者：
Liquidano-Perez, Eduardo [1 ]
Alva-Chaire, Adriana del Carmen [2 ]
Yamazaki-Nakashimada, Marco Antonio [1 ]
Pesantez Abril, Angela Andrea [2 ]
Solorzano Morales, Sara Alejandra [3 ]
Ramirez Ristori, Alfonso G. [4 ]
Barragan Arevalo, Tania [5 ]
Gonzalez-Serrano, Maria Edith [6 ]
Scheffler-Mendoza, Selma C. [1 ]
Rodriguez-Jurado, Rodolfo [2 ,4 ]
机构：
[1] Natl Inst Pediat, Clin Immunol Serv, Mexico City, DF, Mexico
[2] Natl Inst Pediat, Pneumol & Thorax Surg Dept, Mexico City, DF, Mexico
[3] Natl Inst Pediat, Dept Radiol, Mexico City, DF, Mexico
[4] Natl Inst Pediat, Dept Pathol, Insurgentes 3700 C Insurgentes Cuicuilco Coyoca, Mexico City 04530, DF, Mexico
[5] Natl Inst Pediat, Dept Genet, Mexico City, DF, Mexico
[6] Natl Inst Pediat, Immunodeficiency Res Unit, Mexico City, DF, Mexico
来源：
PEDIATRIC ALLERGY AND IMMUNOLOGY | 2022年 / 33卷 / 06期
关键词：
combined immunodeficiency; DOCK8; deficiency; EBV infection; lymphomatoid granulomatosis; lymphoproliferative disorder; INSIGHTS;
D O I：
10.1111/pai.13804
中图分类号：
R392 [医学免疫学];
学科分类号：
100102 ;
摘要：
引用
收藏
页数：5
相关论文
共 50 条
  • [31] Lymphomatoid granulomatosis in a renal transplant patient
    Cachat, F
    Meagher-Villemure, K
    Guignard, JP
    PEDIATRIC NEPHROLOGY, 2003, 18 (08) : 838 - 842
  • [32] Recent Advances in DOCK8 Immunodeficiency Syndrome
    Qian Zhang
    Huie Jing
    Helen C. Su
    Journal of Clinical Immunology, 2016, 36 : 441 - 449
  • [33] Successful treatment of DOCK8 deficiency by allogeneic hematopoietic cell transplantation from alternative donors
    Kono, Asuka
    Wakamatsu, Manabu
    Umezawa, Yoshihiro
    Muramatsu, Hideki
    Fujiwara, Hiroki
    Tomomasa, Dan
    Inoue, Kento
    Hattori, Keiichiro
    Mitsui, Tetsuo
    Takada, Hidetoshi
    Minegishi, Yoshiyuki
    Takahashi, Yoshiyuki
    Yamamoto, Masahide
    Mori, Takehiko
    Kanegane, Hirokazu
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 2023, 118 (04) : 519 - 525
  • [34] DOCK8 Mutation in Patient with Juvenile Idiopathic Arthritis and Sjögren's Syndrome
    Opoka-Winiarska, Violetta
    Winiarska, Natalia
    Lejman, Monika
    Gdak, Malgorzata
    Gosik, Krzysztof
    Lewandowski, Filip
    Niedzwiedzka-Rystwej, Paulina
    Grywalska, Ewelina
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (04)
  • [35] Evaluation of Genotypic Antiviral Resistance Testing as an Alternative to Phenotypic Testing in a Patient with DOCK8 Deficiency and Severe HSV-1 Disease
    Casto, Amanda M.
    Stout, Sean C.
    Selvarangan, Rangaraj
    Freeman, Alexandra F.
    Newell, Brandon D.
    Stahl, Erin D.
    Ahmed, Atif A.
    Greninger, Alexander L.
    Yin, Dwight E.
    JOURNAL OF INFECTIOUS DISEASES, 2020, 221 (12) : 2035 - 2042
  • [36] Hypomorphic DOCK8 deletion causes hypereosinophilic syndrome
    Aryan, Zahra
    Nabavi, Mohammad
    Shabani, Mahsima
    Keles, Sevgi
    Zoghi, Samaneh
    Chatila, Talal
    Rezaei, Nima
    PEDIATRIC BLOOD & CANCER, 2020, 67 (02)
  • [37] DOCK8 Mutation Syndrome: A Diagnostic Challenge for Dermatologists
    Moreau, Josephine
    Beaussant-Cohen, Sarah
    Aubin, Francois
    Rohrlich, Pierre-Simon
    Puzenat, Eve
    ACTA DERMATO-VENEREOLOGICA, 2016, 96 (07) : 991 - 992
  • [38] DOCK8 is critical for the survival and function of NKT cells
    Crawford, Greg
    Enders, Anselm
    Gileadi, Uzi
    Stankovic, Sanda
    Zhang, Qian
    Lambe, Teresa
    Crockford, Tanya L.
    Lockstone, Helen E.
    Freeman, Alexandra
    Arkwright, Peter D.
    Smart, Joanne M.
    Ma, Cindy S.
    Tangye, Stuart G.
    Goodnow, Christopher C.
    Cerundolo, Vincenzo
    Godfrey, Dale I.
    Su, Helen C.
    Randall, Katrina L.
    Cornall, Richard J.
    BLOOD, 2013, 122 (12) : 2052 - 2061
  • [39] Autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency: An adjunctive role for omalizumab
    Kim Han Nguyen
    Quynh Anh Nguyen
    Mai Hoang Tran
    Thu Thuy Can
    Mai Thi Vu
    Nam Sy Vo
    Hieu Chu Chi
    Sheryl van Nunen
    Dinh Van Nguyen
    JOURNAL OF CUTANEOUS IMMUNOLOGY AND ALLERGY, 2022, 5 (06) : 222 - 226
  • [40] LYMPHOMATOID GRANULOMATOSIS
    Dister, F.
    Ghaye, B.
    JBR-BTR, 2012, 95 (03): : 140 - 141
12345