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  1. Article ; Online: Notes on cutaneous manifestations of Kawasaki disease and multisystem inflammatory syndrome in children.

    Gamez-Gonzalez, Luisa Berenise / Ulloa-Gutierrez, Rolando / Yamazaki-Nakashimada, Marco Antonio

    International journal of rheumatic diseases

    2023  Volume 26, Issue 12, Page(s) 2596–2598

    MeSH term(s) Child ; Humans ; Mucocutaneous Lymph Node Syndrome/complications ; Mucocutaneous Lymph Node Syndrome/diagnosis ; Mucocutaneous Lymph Node Syndrome/drug therapy ; Connective Tissue Diseases
    Language English
    Publishing date 2023-07-13
    Publishing country England
    Document type Letter
    ZDB-ID 2426924-4
    ISSN 1756-185X ; 1756-1841
    ISSN (online) 1756-185X
    ISSN 1756-1841
    DOI 10.1111/1756-185X.14821
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    Zs.A 6098: Show issues Location:
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  2. Article ; Online: Cyclosporin for treatment of refractory multisystemic inflammatory syndrome in a child.

    Gámez-González, Luisa Berenise / Hamada, Hiromichi / Yamazaki-Nakashimada, Marco Antonio

    Cardiology in the young

    2022  Volume 33, Issue 5, Page(s) 800–802

    Abstract: Multisystemic inflammatory syndrome in children is an inflammatory condition with multiorgan dysfunction that manifest late in the course of Severe acute respiratory syndrome coronavirus 2 infection. We present a 12-year-old boy with a history of fever, ... ...

    Abstract Multisystemic inflammatory syndrome in children is an inflammatory condition with multiorgan dysfunction that manifest late in the course of Severe acute respiratory syndrome coronavirus 2 infection. We present a 12-year-old boy with a history of fever, vomiting, diarrhoea, and abdominal pain. He developed shock with ventricular dysfunction and pericardial effusion. He was diagnosed with multisystemic inflammatory syndrome in children and treatment with intravenous immunoglobulins, corticosteroids, and tocilizumab proved to be ineffective. Eventually, the patient responded to cyclosporin-A treatment. Multisystemic inflammatory syndrome in children has been treated with immunoglobulins and glucocorticoids and in refractory cases biologics and cyclosporin-A have been used. Intravenous and oral cyclosporin-A seems to be a safe and effective alternative treatment for refractory multisystemic inflammatory syndrome in children patients.
    MeSH term(s) Male ; Humans ; Child ; Cyclosporine ; COVID-19 ; Abdominal Pain ; Administration, Intravenous ; Diarrhea ; Syndrome
    Chemical Substances Cyclosporine (83HN0GTJ6D)
    Language English
    Publishing date 2022-09-02
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 1078466-4
    ISSN 1467-1107 ; 1047-9511
    ISSN (online) 1467-1107
    ISSN 1047-9511
    DOI 10.1017/S1047951122002748
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    Zs.A 4050: Show issues Location:
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  3. Article ; Online: Combined Treatment of Progressive Encephalitis in an X-linked Agammaglobulinemia Patient.

    Yamazaki-Nakashimada, Marco Antonio / Herrera-Mora, Patricia / Mahrx-Bracho, Alfonso / López-Herrera, Gabriela / Bustamante-Ogando, Juan Carlos / Scheffler-Mendoza, Selma Cecilia

    Iranian journal of allergy, asthma, and immunology

    2023  Volume 22, Issue 5, Page(s) 504–509

    Abstract: Most patients with X-linked agammaglobulinemia are susceptible to infections, while some cases also suffer from inflammatory or autoimmune complications. We describe a patient with progressive encephalitis who improved after the use of immunomodulatory ... ...

    Abstract Most patients with X-linked agammaglobulinemia are susceptible to infections, while some cases also suffer from inflammatory or autoimmune complications. We describe a patient with progressive encephalitis who improved after the use of immunomodulatory treatment with corticosteroids, fluoxetine, and nitazoxanide. In most of the cases the evolution of the progressive encephalitis is complicated and catastrophic. Based on our experience and the review of the literature, we propose the use of this combined treatment to control this devastating complication.
    MeSH term(s) Humans ; Genetic Diseases, X-Linked/complications ; Genetic Diseases, X-Linked/diagnosis ; Genetic Diseases, X-Linked/drug therapy ; Encephalitis/complications ; Agammaglobulinemia/complications ; Agammaglobulinemia/diagnosis ; Agammaglobulinemia/drug therapy ; Combined Modality Therapy
    Language English
    Publishing date 2023-10-29
    Publishing country Iran
    Document type Case Reports ; Review ; Journal Article
    ZDB-ID 2488724-9
    ISSN 1735-5249 ; 1735-1502
    ISSN (online) 1735-5249
    ISSN 1735-1502
    DOI 10.18502/ijaai.v22i5.13999
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  4. Article ; Online: Erythema Multiforme: Think Kawasaki Disease.

    Gámez-González, Luisa Berenise / Yamazaki-Nakashimada, Marco Antonio

    Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases

    2019  Volume 26, Issue 6, Page(s) e181–e182

    MeSH term(s) Diagnosis, Differential ; Erythema Multiforme/diagnosis ; Erythema Multiforme/etiology ; Humans ; Mucocutaneous Lymph Node Syndrome/complications ; Mucocutaneous Lymph Node Syndrome/diagnosis
    Language English
    Publishing date 2019-05-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1283266-2
    ISSN 1536-7355 ; 1076-1608
    ISSN (online) 1536-7355
    ISSN 1076-1608
    DOI 10.1097/RHU.0000000000001055
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    Zs.A 4815: Show issues Location:
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  5. Article ; Online: IL-1 receptor antagonist defect (DIRA) in a pediatric patient, receiving adalimumab with good clinical response.

    Bustamante-Ogando, Juan Carlos / Scheffler-Mendoza, Selma / Yamazaki-Nakashimada, Marco Antonio / Saez-de-Ocariz, Marimar

    International journal of dermatology

    2021  Volume 60, Issue 5, Page(s) 639–640

    MeSH term(s) Adalimumab/adverse effects ; Antirheumatic Agents/adverse effects ; Child ; Homozygote ; Humans ; Interleukin 1 Receptor Antagonist Protein ; Receptors, Interleukin-1 ; Tumor Necrosis Factor-alpha
    Chemical Substances Antirheumatic Agents ; Interleukin 1 Receptor Antagonist Protein ; Receptors, Interleukin-1 ; Tumor Necrosis Factor-alpha ; Adalimumab (FYS6T7F842)
    Language English
    Publishing date 2021-01-11
    Publishing country England
    Document type Letter
    ZDB-ID 412254-9
    ISSN 1365-4632 ; 0011-9059 ; 1461-1244
    ISSN (online) 1365-4632
    ISSN 0011-9059 ; 1461-1244
    DOI 10.1111/ijd.15411
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  6. Article ; Online: Therapeutic plasma exchange in refractory macrophage activation syndrome complicating systemic juvenile idiopathic arthritis: a case-based review.

    Liquidano-Perez, Eduardo / Maza-Ramos, Gibert / Salazar-Bailón, José Luis / Yamazaki-Nakashimada, Marco Antonio / Rivas-Larrauri, Francisco

    Rheumatology international

    2022  Volume 43, Issue 1, Page(s) 183–189

    Abstract: Juvenile idiopathic arthritis (JIA) is a heterogeneous group of arthritis of autoimmune aetiology. Systemic-onset juvenile idiopathic arthritis (soJIA) presents with fever, transient erythematous rash, hepatomegaly, splenomegaly, lymphadenopathy, and ... ...

    Abstract Juvenile idiopathic arthritis (JIA) is a heterogeneous group of arthritis of autoimmune aetiology. Systemic-onset juvenile idiopathic arthritis (soJIA) presents with fever, transient erythematous rash, hepatomegaly, splenomegaly, lymphadenopathy, and serositis. SoJIA presents multiple complications, and the most severe is the macrophage activation syndrome (MAS); the timely treatment of MAS must be established early and aggressively to avoid a fatal outcome. Therapeutic plasma exchange has anecdotally been used in refractory cases. A 66-month-old male with a 1-year illness characterized by evening-predominant, intermittent fever, adenomegalies, urticarial-like rash, arthralgia, and arthritis. Biochemical analysis revealed anaemia, leukocytosis, neutrophilia, hypertriglyceridemia, hyperferritinemia, and hypofibrinogenemia; bone marrow aspirate showed hemophagocytosis. He was diagnosed with SoJIA complicated with MAS. He received multiple treatments with IV human gammaglobulin, cyclosporine, dexamethasone, and tocilizumab without improvement. Plasma replacement treatment was performed. Afterwards, he presented significant improvement. After 3-year-follow-up, he remains in good general condition. We present a refractory case of soJIA complicated with MAS successfully treated with plasma exchange.
    MeSH term(s) Humans ; Male ; Child, Preschool ; Arthritis, Juvenile/complications ; Arthritis, Juvenile/therapy ; Arthritis, Juvenile/diagnosis ; Macrophage Activation Syndrome/complications ; Macrophage Activation Syndrome/therapy ; Plasma Exchange/adverse effects ; Lymphohistiocytosis, Hemophagocytic/complications ; Exanthema
    Language English
    Publishing date 2022-10-20
    Publishing country Germany
    Document type Journal Article ; Review
    ZDB-ID 8286-7
    ISSN 1437-160X ; 0172-8172
    ISSN (online) 1437-160X
    ISSN 0172-8172
    DOI 10.1007/s00296-022-05231-z
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    Zs.A 1639: Show issues Location:
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  7. Article ; Online: Periorbital erythema and edema in multisystemic inflammatory syndrome in children, an important diagnostic clue.

    Leon-Perez, Katya Melina / Gamez-Gonzalez, Luisa Berenise / Scheffler-Mendoza, Selma / Mendez-Herrera, Agustín / Lima-Lopez, Asling / Yamazaki-Nakashimada, Marco Antonio

    International journal of rheumatic diseases

    2022  Volume 25, Issue 8, Page(s) 960–961

    MeSH term(s) Child ; Edema/diagnosis ; Edema/etiology ; Erythema/diagnosis ; Erythema/drug therapy ; Erythema/etiology ; Humans ; Syndrome
    Language English
    Publishing date 2022-06-03
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 2426924-4
    ISSN 1756-185X ; 1756-1841
    ISSN (online) 1756-185X
    ISSN 1756-1841
    DOI 10.1111/1756-185X.14350
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  8. Article ; Online: Malar rash in multisystemic inflammatory syndrome in children.

    Moreno-Espinosa, Sarbelio / Rivera-Rodríguez, Leonardo / Gámez-González, Luisa Berenise / Chavez-Priego, Renata / Yamazaki-Nakashimada, Marco Antonio

    Pediatrics international : official journal of the Japan Pediatric Society

    2022  Volume 64, Issue 1, Page(s) e15309

    MeSH term(s) Child ; Humans ; Exanthema/diagnosis ; Exanthema/etiology ; Autoimmune Diseases
    Language English
    Publishing date 2022-10-22
    Publishing country Australia
    Document type Journal Article
    ZDB-ID 1470376-2
    ISSN 1442-200X ; 1328-8067
    ISSN (online) 1442-200X
    ISSN 1328-8067
    DOI 10.1111/ped.15309
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    Zs.A 848: Show issues Location:
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  9. Article ; Online: Clinical manifestations and expression of CD18 to guide the diagnosis of leukocyte adhesion deficiency type 1: Mexico experience.

    Fuentes-Lara, Elma Isela / Arce-Estrada, Gabriel Emmanuel / Bojalil-Cabildo, Abner / Yamazaki-Nakashimada, Marco Antonio / Espinosa-Padilla, Sara Elva / Gamez-Gonzalez, Luisa Berenise / Ramirez-Uribe, Rosa María Nideshda / Saucedo-Ramirez, Omar Josue / Berron-Ruiz, Laura

    Allergologia et immunopathologia

    2023  Volume 51, Issue 6, Page(s) 89–96

    Abstract: Background: Leukocyte adhesion deficiency type 1 (LAD-1) is an inborn error of immunity characterized by a defect in leukocyte trafficking.: Methods: Patients with clinical suspicion of LAD-1 were referred to our institution. Complete blood count and ...

    Abstract Background: Leukocyte adhesion deficiency type 1 (LAD-1) is an inborn error of immunity characterized by a defect in leukocyte trafficking.
    Methods: Patients with clinical suspicion of LAD-1 were referred to our institution. Complete blood count and flow cytometric analysis, to identify the expression of CD18, CD11b, and the lymphocyte population phenotyping, were performed, and statistical analysis was completed.
    Results: We report clinical manifestations and immunological findings of six Mexican patients diagnosed with LAD-1. The diagnosis was based on typical clinical presentation, combined with laboratory demonstration of leukocytosis, and significant reduction or near absence of CD18 and its associated molecules CD11a, CD11b, and CD11c on leukocytes. We found atypical manifestations, not described in other countries, such as early-onset autoimmunity or infections caused by certain microorganisms.
    Conclusions: Patients with LAD-1 may present with atypical manifestations, making flow cytometry an indispensable tool to confirm the diagnosis. We present the first report of LAD-1 patients in a Latin American country.
    MeSH term(s) Humans ; CD18 Antigens/metabolism ; Mexico ; Leukocyte-Adhesion Deficiency Syndrome/diagnosis ; Leukocytes
    Chemical Substances CD18 Antigens
    Language English
    Publishing date 2023-11-01
    Publishing country Singapore
    Document type Journal Article
    ZDB-ID 193144-1
    ISSN 1578-1267 ; 0301-0546
    ISSN (online) 1578-1267
    ISSN 0301-0546
    DOI 10.15586/aei.v51i6.914
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    Zs.A 1165: Show issues Location:
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  10. Article ; Online: Erythema and Induration at BCG Site in IPEX Syndrome.

    Castano-Jaramillo, Lina Maria / Toledo-Salinas, Carla / Saez-de-Ocariz, Maria Del Mar / Toussaint-Caire, Sonia / Bustamante Ogando, Juan Carlos / Rivas-Larrauri, Francisco / Scheffler-Mendoza, Selma / Yamazaki-Nakashimada, Marco Antonio

    Indian journal of dermatology

    2023  Volume 67, Issue 5, Page(s) 617–619

    Language English
    Publishing date 2023-01-30
    Publishing country India
    Document type Journal Article
    ZDB-ID 416069-1
    ISSN 1998-3611 ; 0019-5154
    ISSN (online) 1998-3611
    ISSN 0019-5154
    DOI 10.4103/ijd.ijd_973_21
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