Adrenal Medullary Hyperplasia: An Under the Radar Cause of Endocrine Hypertension

被引:4
作者
Mejia, Ana M. Rivas [1 ]
Cameselle-Teijeiro, Jose M. [2 ]
Thavaraputta, Subhanudh [3 ]
Lado-Abeal, Joaquin [4 ]
机构
[1] Texas Tech Univ, Dept Internal Med, Div Endocrinol, Hlth Sci Ctr,Sch Med, Lubbock, TX 79430 USA
[2] Univ Santiago de Compostela, Clin Univ Hosp, Dept Pathol, Galician Healthcare Serv SERGAS,FIDIS, Travesia Choupana S-N, Santiago De Compostela 15706, Spain
[3] Texas Tech Univ, Dept Internal Med, Hlth Sci Ctr, Sch Med, Lubbock, TX 79430 USA
[4] Univ Missouri, Truman Med Ctr, Dept Internal Med, Div Endocrinol, Kansas City, MO USA
关键词
PHEOCHROMOCYTOMA; MUTATIONS; RET;
D O I
10.1016/j.amjms.2020.06.031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adrenal medullary hyperplasia is a cause of increased secretion of catecholamines by the adrenal gland that is rarely considered among the differential diagnoses of endocrine hypertension. We report the case of a 48-year-old Hispanic woman who presented for evaluation of resistant hypertension with several episodes of hypertensive crisis. The clinical presentation, biochemical results, and abdominal computed tomography scan suggested the possibility of a pheochromocytoma; however, an iodine-123-meta-iodobenzylguanidine (I-123-MIBG) uptake study combined with single-photon emission computed tomography (SPECT) and computed tomography (CT) scan showed diffusely increased metabolic activity in both adrenal glands. The patient underwent left adrenalectomy, and the pathology study revealed the presence of adrenal medullary hyperplasia. After surgery, blood pressure control was achieved with one antihypertensive drug, and the patient did not have recurrent hypertensive crisis. Relevant findings obtained from a whole genomic sequence done on a whole blood DNA sample from the patient are discussed.
引用
收藏
页码:64 / 68
页数:5
相关论文
共 21 条
[1]  
[Anonymous], 2017, WHO Classification of Tumours of Endocrine Organs
[2]   HYPERPLASIA OF ADRENAL MEDULLA IN HYPERTENSION OF CHILDREN [J].
BIALESTOCK, D .
ARCHIVES OF DISEASE IN CHILDHOOD, 1961, 36 (189) :465-+
[3]  
CARNEY JA, 1976, AM J CLIN PATHOL, V66, P279
[4]   Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas [J].
Castro-Vega, Luis Jaime ;
Letouze, Eric ;
Burnichon, Nelly ;
Buffet, Alexandre ;
Disderot, Pierre-Helie ;
Khalifa, Emmanuel ;
Loriot, Celine ;
Elarouci, Nabila ;
Morin, Aurelie ;
Menara, Melanie ;
Lepoutre-Lussey, Charlotte ;
Badoual, Cecile ;
Sibony, Mathilde ;
Dousset, Bertrand ;
Libe, Rossella ;
Zinzindohoue, Franck ;
Plouin, Pierre Francois ;
Bertherat, Jerome ;
Amar, Laurence ;
de Reynies, Aurelien ;
Favier, Judith ;
Gimenez-Roqueplo, Anne-Paule .
NATURE COMMUNICATIONS, 2015, 6
[5]   Traditional and targeted exome sequencing reveals common, rare and novel functional deleterious variants in RET-signaling complex in a cohort of living US patients with urinary tract malformations [J].
Chatterjee, Rajshekhar ;
Ramos, Enrique ;
Hoffman, Mary ;
VanWinkle, Jessica ;
Martin, Daniel R. ;
Davis, Thomas K. ;
Hoshi, Masato ;
Hmiel, Stanley P. ;
Beck, Anne ;
Hruska, Keith ;
Coplen, Doug ;
Liapis, Helen ;
Mitra, Robi ;
Druley, Todd ;
Austin, Paul ;
Jain, Sanjay .
HUMAN GENETICS, 2012, 131 (11) :1725-1738
[6]   HYPERPLASIA OF THE ADRENAL MEDULLA [J].
DRUKKER, W ;
FORMIJNE, P ;
VANDERSCHOOT, JB .
BMJ-BRITISH MEDICAL JOURNAL, 1957, 1 (JAN26) :186-+
[7]   Presentation, Treatment, Histology, and Outcomes in Adrenal Medullary Hyperplasia Compared With Pheochromocytoma [J].
Falhammar, Henrik ;
Stenman, Adam ;
Calissendorff, Jan ;
Juhlin, Carl Christofer .
JOURNAL OF THE ENDOCRINE SOCIETY, 2019, 3 (08) :1518-1530
[8]   Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma [J].
Fishbein, Lauren ;
Leshchiner, Ignaty ;
Walter, Vonn ;
Danilova, Ludmila ;
Robertson, A. Gordon ;
Johnson, Amy R. ;
Lichtenberg, Tara M. ;
Murray, Bradley A. ;
Ghayee, Hans K. ;
Else, Tobias ;
Ling, Shiyun ;
Jefferys, Stuart R. ;
de Cubas, Aguirre A. ;
Wenz, Brandon ;
Korpershoek, Esther ;
Amelio, Antonio L. ;
Makowski, Liza ;
Rathmell, W. Kimryn ;
Gimenez-Roqueplo, Anne-Paule ;
Giordano, Thomas J. ;
Asa, Sylvia L. ;
Tischler, Arthur S. ;
Pacak, Karel ;
Nathanson, Katherine L. ;
Wilkerson, Matthew D. .
CANCER CELL, 2017, 31 (02) :181-193
[9]   Mastermind-Like 3 Controls Proliferation and Differentiation in Neuroblastoma [J].
Heynen, Guus J. J. E. ;
Nevedomskaya, Ekaterina ;
Palit, Sander ;
Basheer, Noorjahan Jagalur ;
Lieftink, Cor ;
Schlicker, Andreas ;
Zwart, Wilbert ;
Bernards, Rene ;
Bajpe, Prashanth Kumar .
MOLECULAR CANCER RESEARCH, 2016, 14 (05) :411-422
[10]   RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects [J].
Jeanpierre, Cecile ;
Mace, Guillaume ;
Parisot, Melanie ;
Moriniere, Vincent ;
Pawtowsky, Audrey ;
Benabou, Marion ;
Martinovic, Jelena ;
Amiel, Jeanne ;
Attie-Bitach, Tania ;
Delezoide, Anne-Lise ;
Loget, Philippe ;
Blanchet, Patricia ;
Gaillard, Dominique ;
Gonzales, Marie ;
Carpentier, Wassila ;
Nitschke, Patrick ;
Tores, Frederic ;
Heidet, Laurence ;
Antignac, Corinne ;
Salomon, Remi .
JOURNAL OF MEDICAL GENETICS, 2011, 48 (07) :497-504