Case Report: Severe Hypocalcemic Episodes Due to Autoimmune Enteropathy

被引:5
作者
Halabi, Inbal [1 ,2 ]
Barohom, Marie Noufi [1 ,2 ,3 ]
Peleg, Sarit [4 ]
Trougouboff, Phillippe [5 ]
Elias-Assad, Ghadir [1 ,6 ]
Agbaria, Rhania [7 ]
Tenenbaum-Rakover, Yardena [1 ,6 ]
机构
[1] HaEmek Med Ctr, Pediat Endocrine Inst, Afula, Israel
[2] Clalit Hlth Serv, Pediat Hlth Ctr, Nahariyya, Israel
[3] Bar Ilan Univ, Fac Med, Safed, Israel
[4] Clalit Hlth Serv, Pediat Hlth Ctr, Hadera, Israel
[5] HaEmek Med Ctr, Tissue Diag & Canc Res Dept, Afula, Israel
[6] Technion, Ruth & Bruce Rappaport Fac Med, Haifa, Israel
[7] HaEmek Med Ctr, Pediat Gastroenterol Unit, Afula, Israel
关键词
autoimmune polyglandular type 1 syndrome; autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy; autoimmune regulator gene; autoimmune enteropathy; hypocalcemia; enteroendocrine cell; chromogranin A; CANDIDIASIS-ECTODERMAL DYSTROPHY; ENTEROENDOCRINE CELLS; TRYPTOPHAN-HYDROXYLASE; ENDOCRINE-CELLS; CHOLECYSTOKININ; AUTOANTIBODIES; MANIFESTATIONS; MALABSORPTION; MUTATION; PATIENT;
D O I
10.3389/fendo.2021.645279
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a rare monogenic disorder, associated with endocrine deficiencies and non-endocrine involvement. Gastrointestinal (GI) manifestations appear in approximately 25% of patients and are the presenting symptom in about 10% of them. Limited awareness among pediatricians of autoimmune enteropathy (AIE) caused by destruction of the gut endocrine cells in APECED patients delays diagnosis and appropriate therapy. We describe an 18-year-old female presenting at the age of 6.10 years with hypoparathyroidism, oral candidiasis and vitiligo. The clinical diagnosis of APECED was confirmed by sequencing the autoimmune regulator-encoding (AIRE) gene. Several characteristics of the disease-Hashimoto's thyroiditis, Addison's disease, diabetes mellitus type 1 and primary ovarian insufficiency-developed over the years. She had recurrent episodes of severe intractable hypocalcemia. Extensive GI investigations for possible malabsorption, including laboratory analyses, imaging and endoscopy with biopsies were unremarkable. Revision of the biopsies and chromogranin A (CgA) immunostaining demonstrated complete loss of enteroendocrine cells in the duodenum and small intestine, confirming the diagnosis of AIE. Management of hypocalcemia was challenging. Only intravenous calcitriol maintained calcium in the normal range. Between hypocalcemic episodes, the proband maintained normal calcium levels, suggesting a fluctuating disease course. Repeated intestinal biopsy revealed positive intestinal CgA immunostaining. The attribution of severe hypocalcemic episodes to AIE emphasizes the need for increased awareness of this unique presentation of APECED. The fluctuating disease course and repeated intestinal biopsy showing positive CgA immunostaining support a reversible effect of GI involvement. CgA immunostaining is indicated in patients with APECED for whom all other investigations have failed to reveal an explanation for the malabsorption.
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页数:8
相关论文
共 32 条
[1]   CLINICAL VARIATION OF AUTOIMMUNE POLYENDOCRINOPATHY CANDIDIASIS ECTODERMAL DYSTROPHY (APECED) IN A SERIES OF 68 PATIENTS [J].
AHONEN, P ;
MYLLARNIEMI, S ;
SIPILA, I ;
PERHEENTUPA, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (26) :1829-1836
[2]   Projection of an immunological self shadow within the thymus by the aire protein [J].
Anderson, MS ;
Venanzi, ES ;
Klein, L ;
Chen, ZB ;
Berzins, SP ;
Turley, SJ ;
von Boehmer, H ;
Bronson, R ;
Dierich, A ;
Benoist, C ;
Mathis, D .
SCIENCE, 2002, 298 (5597) :1395-1401
[3]   Intravenous versus oral vitamin D therapy in dialysis patients: What is the question? [J].
Andress, DL .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 38 (05) :S41-S44
[4]  
BARRETT P, 1995, HISTOCHEM J, V27, P482
[5]   Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy: Insights into Genotype-Phenotype Correlation [J].
Capalbo, Donatella ;
De Martino, Lucia ;
Giardino, Giuliana ;
Di Mase, Raffaella ;
Di Donato, Iolanda ;
Parenti, Giancarlo ;
Vajro, Pietro ;
Pignata, Claudio ;
Salerno, Mariacarolina .
INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2012, 2012
[6]   Novel AIRE mutations and P450 cytochrome autoantibodies in Central and Eastern European patients with APECED [J].
Cihakova, D ;
Trebusak, K ;
Heino, M ;
Fadeyev, V ;
Tiulpakov, A ;
Battelino, T ;
Tar, A ;
Halász, Z ;
Blümel, P ;
Tawfik, S ;
Krohn, K ;
Lebl, J ;
Peterson, P .
HUMAN MUTATION, 2001, 18 (03) :225-232
[7]  
Di Maio Salvatore, 2018, Acta Biomed, V89, P122, DOI 10.23750/abm.v89i1.7118
[8]   Identification of tryptophan hydroxylase as an intestinal autoantigen [J].
Ekwall, O ;
Hedstrand, H ;
Grimelius, L ;
Haavik, J ;
Perheentupa, J ;
Gustafsson, J ;
Husebye, E ;
Kämpe, O ;
Rorsman, F .
LANCET, 1998, 352 (9124) :279-283
[9]   Tryptophan hydroxylase autoantibodies and intestinal disease in autoimmune polyendocrine syndrome type 1 [J].
Ekwall, O ;
Sjöberg, K ;
Mirakian, R ;
Rorsman, F ;
Kämpe, O .
LANCET, 1999, 354 (9178) :568-568
[10]   Redefined clinical features and diagnostic criteria in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy [J].
Ferre, Elise M. N. ;
Rose, Stacey R. ;
Rosenzweig, Sergio D. ;
Burbelo, Peter D. ;
Romito, Kimberly R. ;
Niemela, Julie E. ;
Rosen, Lindsey B. ;
Break, Timothy J. ;
Gu, Wenjuan ;
Hunsberger, Sally ;
Browne, Sarah K. ;
Hsu, Amy P. ;
Rampertaap, Shakuntala ;
Swamydas, Muthulekha ;
Collar, Amanda L. ;
Kong, Heidi H. ;
Lee, Chyi-Chia Richard ;
Chascsa, David ;
Simcox, Thomas ;
Pham, Angela ;
Bondici, Anamaria ;
Natarajan, Mukil ;
Monsale, Joseph ;
Kleiner, David E. ;
Quezado, Martha ;
Alevizos, Ilias ;
Moutsopoulos, Niki M. ;
Yockey, Lynne ;
Frein, Cathleen ;
Soldatos, Ariane ;
Calvo, Katherine R. ;
Adjemian, Jennifer ;
Similuk, Morgan N. ;
Lang, David M. ;
Stone, Kelly D. ;
Uzel, Gulbu ;
Kopp, Jeffrey B. ;
Bishop, Rachel J. ;
Holland, Steven M. ;
Olivier, Kenneth N. ;
Fleisher, Thomas A. ;
Heller, Theo ;
Winer, Karen K. ;
Lionakis, Michail S. .
JCI INSIGHT, 2016, 1 (13)