Literature DB >> 12269656

Panhypopituitarism in a child with common variable immunodeficiency.

Jihad S Younes1, Elizabeth A Secord.   

Abstract

BACKGROUND: Common variable immunodeficiency (CVID) represents a group of heterogeneous, still undifferentiated, syndromes that are all characterized by defective antibody formation. It is often associated with autoimmune disease.
METHODS: An African-American girl was diagnosed with CVID at age 3 years. She was seen during an adrenal crisis precipitated by pneumonia at the age of 8 years and 10 months. The diagnosis of panhypopituitarism was established soon after.
RESULTS: Panhypopituitarism in this patient was believed to be the result of the autoimmune process known as lymphocytic hypophysitis. This hypothesis was suggested by the results of magnetic resonance imaging.
CONCLUSIONS: Awareness of the possibility of this process in children or adults with CVID may lead to earlier diagnosis of panhypopituitarism. These patients also have failure to thrive, and earlier diagnosis may avoid a life-threatening event.

Entities:  

Mesh:

Year:  2002        PMID: 12269656     DOI: 10.1016/S1081-1206(10)61963-1

Source DB:  PubMed          Journal:  Ann Allergy Asthma Immunol        ISSN: 1081-1206            Impact factor:   6.347


  7 in total

1.  Partial central diabetes insipidus in patient with common variable immunodeficiency.

Authors:  Marta Cano Megías; Ana Maria Matei; Olga Gonzalez Albarran; Gilberto Perez Lopez
Journal:  BMJ Case Rep       Date:  2012-07-03

Review 2.  Lymphocytic hypophysitis in the pediatric population.

Authors:  Verena Gellner; Senta Kurschel; Michael Scarpatetti; Michael Mokry
Journal:  Childs Nerv Syst       Date:  2008-02-26       Impact factor: 1.475

3.  Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency.

Authors:  Karin Chen; Emily M Coonrod; Attila Kumánovics; Zechariah F Franks; Jacob D Durtschi; Rebecca L Margraf; Wilfred Wu; Nahla M Heikal; Nancy H Augustine; Perry G Ridge; Harry R Hill; Lynn B Jorde; Andrew S Weyrich; Guy A Zimmerman; Adi V Gundlapalli; John F Bohnsack; Karl V Voelkerding
Journal:  Am J Hum Genet       Date:  2013-10-17       Impact factor: 11.025

4.  Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies.

Authors:  Thierry Brue; Marie-Hélène Quentien; Konstantin Khetchoumian; Marco Bensa; José-Mario Capo-Chichi; Brigitte Delemer; Aurelio Balsalobre; Christina Nassif; Dimitris T Papadimitriou; Anne Pagnier; Caroline Hasselmann; Lysanne Patry; Jeremy Schwartzentruber; Pierre-François Souchon; Shinobu Takayasu; Alain Enjalbert; Guy Van Vliet; Jacek Majewski; Jacques Drouin; Mark E Samuels
Journal:  BMC Med Genet       Date:  2014-12-19       Impact factor: 2.103

5.  Deficit of Anterior Pituitary Function and Variable Immune Deficiency Syndrome: A Novel Mutation.

Authors:  Pavadee Poowuttikul; Eric McGrath; Deepak Kamat
Journal:  Glob Pediatr Health       Date:  2017-01-27

6.  Common variable immune deficiency, central diabetes insipidus, and anemia.

Authors:  Marta Baleva; Spaska Lesichkova; Nevena Gesheva; Snejina Mihailova; Vanya Gerova; Borislav Vladimirov; Plamen Penchev; Milena Nikolova-Vlahova; Elissaveta Naumova
Journal:  Cent Eur J Immunol       Date:  2020-11-01       Impact factor: 2.085

7.  Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies.

Authors:  Eva C Coopmans; Paweena Chunharojrith; Sebastian J C M M Neggers; Marianne W van der Ent; Sigrid M A Swagemakers; Iris H Hollink; Barbara H Barendregt; Peter J van der Spek; Aart-Jan van der Lely; P Martin van Hagen; Virgil A S H Dalm
Journal:  Front Immunol       Date:  2019-08-30       Impact factor: 7.561

  7 in total

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