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Case Report
Open Access

oa

Fish Tank Granuloma Presenting as a Nasal Cavity Mass
Motoki Sekine, Fumiyuki Goto, Kosuke Saito, Shoji Kaneda, Hikaru Yamamoto, Tomoaki Murakami, Takahide Hamano, Kenji Okami,

First published: 12 January 2021
Case Report
Open Access

oa

Severe Combined Immunodeficiency Disorder due to a Novel Mutation in Recombination Activation Gene 2: About 2 Cases
Ibtihal Benhsaien, Fatima Ailal, Khadija Elazhary, Jalila El bakkouri, Abdallah Badou, Ahmed Aziz Bousfiha,

First published: 07 January 2021
Case Report
Open Access

oa

Mendelian Susceptibility to Mycobacterial Disease: The First Case of a Diagnosed Adult Patient in the Czech Republic
Miroslav Prucha, Hana Grombirikova, Pavel Zdrahal, Marketa Bloomfield, Zuzana Parackova, Tomas Freiberger,

First published: 21 December 2020
Case Report
Open Access

oa

On Two Cases with Autosomal Dominant Hyper IgE Syndrome: Importance of Immunological Parameters for Clinical Course and Follow-Up
Snezhina Mihailova Kandilarova, Spaska Stoyneva Lesichkova, Nevena Todorova Gesheva, Petya Stefanova Yankova, Nedelcho Hristov Ivanov, Guergana Petrova Stoyanova, Penka Ilieva Perenovska, Marta Petrova Baleva, Elissaveta Jordanova Naumova,

First published: 03 December 2020
Case Report
Open Access

oa

Adverse Events of the BCG (Bacillus Calmette–Guérin) and Rotavirus Vaccines in a Young Infant with Inborn Error of Immunity
Suleiman Al-Hammadi, Najla S. Alkuwaiti, Ghassan A. Ghatasheh, Huda Al Dhanhani, Hiba M. Shendi, Abdulghani S. Elomami, Farida Almarzooqi, Abdul-Kader Souid,

First published: 28 November 2020
Case Report
Open Access

oa

A Case of Prolonged Catatonia Caused by Sjögren’s Syndrome
Takahiko Inagaki, Kotaro Kudo, Naoki Kurimoto, Takashi Aoki, Kenichi Kuriyama,

First published: 03 November 2020
Case Report
Open Access

oa

Interleukin-1 Receptor-Associated Kinase 4 Deficiency in a Greek Teenager
Panagiota Karananou, Anastasia Alataki, Efimia Papadopoulou-Alataki,

First published: 08 October 2020
Case Report
Open Access

oa

IPEX Syndrome with Normal FOXP3 Protein Expression in Treg Cells in an Infant Presenting with Intractable Diarrhea as a Single Symptom
Ali Al Maawali, Beata Derfalvi, Johan Van Limbergen, Andrew Issekutz, Thomas Issekutz, Hasan Ghandourah, Mohsin Rashid,

First published: 09 September 2020
Case Report
Open Access

oa

A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature
Aysun Ata, Samim Özen, Damla Gökşen, Neslihan Edeer Karaca, Güzide Aksu, Necil Kütükçüler, Hüseyin Onay, Şükran Darcan,

First published: 01 September 2020
Case Report
Open Access

oa

The Natural History of X-Linked Lymphoproliferative Disease (XLP1): Lessons from a Long-Term Survivor
Yike Jiang, Mihail Firan, Sarada L. Nandiwada, Anaid Reyes, Rebecca A. Marsh, Tiphanie P. Vogel, Joud Hajjar,

First published: 27 August 2020
Case Report
Open Access

oa

The Terrible Triad of Checkpoint Inhibition: A Case Report of Myasthenia Gravis, Myocarditis, and Myositis Induced by Cemiplimab in a Patient with Metastatic Cutaneous Squamous Cell Carcinoma
Nikeshan Jeyakumar, Mikel Etchegaray, Jason Henry, Laura Lelenwa, Bihong Zhao, Ana Segura, L. Maximilian Buja,

First published: 04 July 2020
Case Report
Open Access

oa

Injection Site Erythema in a Patient on Therapeutic Anticoagulation with Low Molecular Weight Heparin after Mechanical Aortic Valve Replacement: A Rare Presentation of Heparin- and Protamine-Induced Thrombocytopenia
Caroline Holaubek, Paul Simon, Sabine Eichinger-Hasenauer, Franz Gremmel, Barbara Steinlechner,

First published: 10 April 2020
Case Report
Open Access

oa

A First Case Report of DiGeorge Syndrome from Ethiopia Highlights Challenges in Identifying and Treating Children with Primary T-Cell Deficiencies in Low Resource Settings
Tinsae Alemayehu, Solomie Jebessa Deribessa,

First published: 26 February 2020
Case Report
Open Access

oa

Posttransplantation Lymphoproliferative Disease Treated by Retransplantation
Ingerid Weum Abrahamsen, Bjørn Christer Grønvold, Else Marit Inderberg, Nadia Mensali, Jonas Mattsson, Tobias Gedde-Dahl,

First published: 25 February 2020
Case Report
Open Access

oa

Cerebellar Ataxia Followed by Stiff Person Syndrome in a Patient with Anti-GAD Antibodies
Sinali O. Seneviratne, Katherine A. Buzzard, Belinda Cruse, Mastura Monif,

First published: 08 February 2020
Case Report
Open Access

oa

Fatal Hypogammaglobulinemia 3 Years after Rituximab in a Patient with Immune Thrombocytopenia: An Underlying Genetic Predisposition?
Jean-François Viallard, Marie Parrens, Frédéric Rieux-Laucat,

First published: 28 December 2019
Case Report
Open Access

oa

Primary Immunodeficiency with Severe Multi-Organ Immune Dysregulation
Tatyana Gavrilova,

First published: 28 December 2019
Case Report
Open Access

oa

Sirolimus for the Treatment of Airway Obstruction due to Indolent T-Lymphoblastic Proliferation
Eric Moughames, Ana P. Kiess, Lee M. Akst, Antoine Azar,

First published: 16 December 2019
Case Report
Open Access

oa

Evidence that a STAT3 Mutation Causing Hyper IgE Syndrome Leads to Repression of Transcriptional Activity
Sameer Bahal, Maha E. Houssen, Ania Manson, Lorena Lorenzo, Mark A. Russell, Noel G. Morgan, Fariba Tahami, Sofia Grigoriadou,

First published: 13 October 2019
Case Report
Open Access

oa

Deficiency of Interleukin-1 Receptor Antagonist: A Case with Late Onset Severe Inflammatory Arthritis, Nail Psoriasis with Onychomycosis and Well Responsive to Adalimumab Therapy
Necil Kutukculer, Anne Puel, Sanem Eren Akarcan, Kunihiko Moriya, Neslihan Edeer Karaca, Melanie Migaud, Jean-Laurent Casanova, Guzide Aksu,

First published: 04 August 2019

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Case Reports in Immunology

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All Case Reports in Immunology Articles

oa

Fish Tank Granuloma Presenting as a Nasal Cavity Mass

oa

Severe Combined Immunodeficiency Disorder due to a Novel Mutation in Recombination Activation Gene 2: About 2 Cases

oa

Mendelian Susceptibility to Mycobacterial Disease: The First Case of a Diagnosed Adult Patient in the Czech Republic

oa

On Two Cases with Autosomal Dominant Hyper IgE Syndrome: Importance of Immunological Parameters for Clinical Course and Follow-Up

oa

Adverse Events of the BCG (Bacillus Calmette–Guérin) and Rotavirus Vaccines in a Young Infant with Inborn Error of Immunity

oa

A Case of Prolonged Catatonia Caused by Sjögren’s Syndrome

oa

Interleukin-1 Receptor-Associated Kinase 4 Deficiency in a Greek Teenager

oa

IPEX Syndrome with Normal FOXP3 Protein Expression in Treg Cells in an Infant Presenting with Intractable Diarrhea as a Single Symptom

oa

A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature

oa

The Natural History of X-Linked Lymphoproliferative Disease (XLP1): Lessons from a Long-Term Survivor

oa

The Terrible Triad of Checkpoint Inhibition: A Case Report of Myasthenia Gravis, Myocarditis, and Myositis Induced by Cemiplimab in a Patient with Metastatic Cutaneous Squamous Cell Carcinoma

oa

Injection Site Erythema in a Patient on Therapeutic Anticoagulation with Low Molecular Weight Heparin after Mechanical Aortic Valve Replacement: A Rare Presentation of Heparin- and Protamine-Induced Thrombocytopenia

oa

A First Case Report of DiGeorge Syndrome from Ethiopia Highlights Challenges in Identifying and Treating Children with Primary T-Cell Deficiencies in Low Resource Settings

oa

Posttransplantation Lymphoproliferative Disease Treated by Retransplantation

oa

Cerebellar Ataxia Followed by Stiff Person Syndrome in a Patient with Anti-GAD Antibodies

oa

Fatal Hypogammaglobulinemia 3 Years after Rituximab in a Patient with Immune Thrombocytopenia: An Underlying Genetic Predisposition?

oa

Primary Immunodeficiency with Severe Multi-Organ Immune Dysregulation

oa

Sirolimus for the Treatment of Airway Obstruction due to Indolent T-Lymphoblastic Proliferation

oa

Evidence that a STAT3 Mutation Causing Hyper IgE Syndrome Leads to Repression of Transcriptional Activity

oa

Deficiency of Interleukin-1 Receptor Antagonist: A Case with Late Onset Severe Inflammatory Arthritis, Nail Psoriasis with Onychomycosis and Well Responsive to Adalimumab Therapy

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oa Fish Tank Granuloma Presenting as a Nasal Cavity Mass

oa Severe Combined Immunodeficiency Disorder due to a Novel Mutation in Recombination Activation Gene 2: About 2 Cases

oa Mendelian Susceptibility to Mycobacterial Disease: The First Case of a Diagnosed Adult Patient in the Czech Republic

oa On Two Cases with Autosomal Dominant Hyper IgE Syndrome: Importance of Immunological Parameters for Clinical Course and Follow-Up

oa Adverse Events of the BCG (Bacillus Calmette–Guérin) and Rotavirus Vaccines in a Young Infant with Inborn Error of Immunity

oa A Case of Prolonged Catatonia Caused by Sjögren’s Syndrome

oa Interleukin-1 Receptor-Associated Kinase 4 Deficiency in a Greek Teenager

oa IPEX Syndrome with Normal FOXP3 Protein Expression in Treg Cells in an Infant Presenting with Intractable Diarrhea as a Single Symptom

oa A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature

oa The Natural History of X-Linked Lymphoproliferative Disease (XLP1): Lessons from a Long-Term Survivor

oa The Terrible Triad of Checkpoint Inhibition: A Case Report of Myasthenia Gravis, Myocarditis, and Myositis Induced by Cemiplimab in a Patient with Metastatic Cutaneous Squamous Cell Carcinoma

oa Injection Site Erythema in a Patient on Therapeutic Anticoagulation with Low Molecular Weight Heparin after Mechanical Aortic Valve Replacement: A Rare Presentation of Heparin- and Protamine-Induced Thrombocytopenia

oa A First Case Report of DiGeorge Syndrome from Ethiopia Highlights Challenges in Identifying and Treating Children with Primary T-Cell Deficiencies in Low Resource Settings

oa Posttransplantation Lymphoproliferative Disease Treated by Retransplantation

oa Cerebellar Ataxia Followed by Stiff Person Syndrome in a Patient with Anti-GAD Antibodies

oa Fatal Hypogammaglobulinemia 3 Years after Rituximab in a Patient with Immune Thrombocytopenia: An Underlying Genetic Predisposition?

oa Primary Immunodeficiency with Severe Multi-Organ Immune Dysregulation

oa Sirolimus for the Treatment of Airway Obstruction due to Indolent T-Lymphoblastic Proliferation

oa Evidence that a STAT3 Mutation Causing Hyper IgE Syndrome Leads to Repression of Transcriptional Activity

oa Deficiency of Interleukin-1 Receptor Antagonist: A Case with Late Onset Severe Inflammatory Arthritis, Nail Psoriasis with Onychomycosis and Well Responsive to Adalimumab Therapy

oa

Fish Tank Granuloma Presenting as a Nasal Cavity Mass

oa

Severe Combined Immunodeficiency Disorder due to a Novel Mutation in Recombination Activation Gene 2: About 2 Cases

oa

Mendelian Susceptibility to Mycobacterial Disease: The First Case of a Diagnosed Adult Patient in the Czech Republic

oa

On Two Cases with Autosomal Dominant Hyper IgE Syndrome: Importance of Immunological Parameters for Clinical Course and Follow-Up

oa

Adverse Events of the BCG (Bacillus Calmette–Guérin) and Rotavirus Vaccines in a Young Infant with Inborn Error of Immunity

oa

A Case of Prolonged Catatonia Caused by Sjögren’s Syndrome

oa

Interleukin-1 Receptor-Associated Kinase 4 Deficiency in a Greek Teenager

oa

IPEX Syndrome with Normal FOXP3 Protein Expression in Treg Cells in an Infant Presenting with Intractable Diarrhea as a Single Symptom

oa

A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature

oa

The Natural History of X-Linked Lymphoproliferative Disease (XLP1): Lessons from a Long-Term Survivor

oa

The Terrible Triad of Checkpoint Inhibition: A Case Report of Myasthenia Gravis, Myocarditis, and Myositis Induced by Cemiplimab in a Patient with Metastatic Cutaneous Squamous Cell Carcinoma

oa

Injection Site Erythema in a Patient on Therapeutic Anticoagulation with Low Molecular Weight Heparin after Mechanical Aortic Valve Replacement: A Rare Presentation of Heparin- and Protamine-Induced Thrombocytopenia

oa

A First Case Report of DiGeorge Syndrome from Ethiopia Highlights Challenges in Identifying and Treating Children with Primary T-Cell Deficiencies in Low Resource Settings

oa

Posttransplantation Lymphoproliferative Disease Treated by Retransplantation

oa

Cerebellar Ataxia Followed by Stiff Person Syndrome in a Patient with Anti-GAD Antibodies

oa

Fatal Hypogammaglobulinemia 3 Years after Rituximab in a Patient with Immune Thrombocytopenia: An Underlying Genetic Predisposition?

oa

Primary Immunodeficiency with Severe Multi-Organ Immune Dysregulation

oa

Sirolimus for the Treatment of Airway Obstruction due to Indolent T-Lymphoblastic Proliferation

oa

Evidence that a STAT3 Mutation Causing Hyper IgE Syndrome Leads to Repression of Transcriptional Activity

oa

Deficiency of Interleukin-1 Receptor Antagonist: A Case with Late Onset Severe Inflammatory Arthritis, Nail Psoriasis with Onychomycosis and Well Responsive to Adalimumab Therapy