Öz
Giriş
Hiperkalsemi çocuklarda yetişkinlere kıyasla daha nadir görülmekle birlikte, klinik olarak önemli bir durumdur.
Gereç ve Yöntem
Bu retrospektif çalışmada hiperkalsemi saptanan 0–18 yaş arası 21 hasta değerlendirildi. Klinik özellikler, laboratuvar bulguları ile klinik gerekliliğe göre yapılan görüntüleme ve genetik analizler incelendi. Hastalar hiperkalsemi şiddeti ve PTH durumuna göre sınıflandırılarak tedavi sonuçları kaydedildi.
Bulgular
Hastaların %33,3’ü asemptomatikti ve en sık başvuru şikâyeti kusmaydı (%19). Hastaların %66,7’sinde paratiroid hormonuna (PTH) bağımsız hiperkalsemi saptanırken, %33,3’ünde PTH’ye bağlı hiperkalsemi mevcuttu. Saptanan etiyolojiler arasında beş hastada paratiroid adenom, dört hastada adrenal yetmezlik, üç hastada D vitamini intoksikasyonu, üç hastada malignite, birer hastada osteomiyelit, psödohipoaldosteronizm, CaSR varyantı ve hipofosfatazya yer almaktadır. PTH’ye bağlı hiperkalsemisi olan yedi hastadan dördü cerrahi tedavi almıştır.
Sonuç
Bu çalışma, çocukluk çağı hiperkalsemisinin çok çeşitli nedenlere bağlı olarak gelişebileceğini ortaya koymaktadır. Belirsiz veya spesifik olmayan klinik bulgularla başvuran çocuklarda serum kalsiyum düzeylerinin ölçülmesi büyük önem taşımaktadır. Ek bulguların yokluğunda malignite tanısı gecikebilir. Erken tanı ve uygun müdahale, ciddi komplikasyonların önlenmesine katkı sağlayabilir.
Anahtar Kelimeler: Etiyoloji, hiperkalsemi, malignite, paratiroid hormon, pediatrik
Kaynakça
McNeilly JD, Boal R, Shaikh MG, Ahmed SF. Frequency and aetiology of hypercalcaemia. Arch Dis Child. 2016;101:344-7.
Stokes VJ, Nielsen MF, Hannan FM, Thakker RV. Hypercalcemic disorders in children. J Bone Miner Res. 2017;32:2157-70.
Darendeliler F, Aycan Z, Kara C, Özen S, Eren E. Çocuk endokrinolojisi ve diyabet. İstanbul Tıp Kitabevleri. 2021:1776.
Davies JH. Approach to the child with hypercalcaemia. Endocr Dev. 2015;28:101-18.
Davies JH, Shaw NJ. Investigation and management of hypercalcaemia in children. Arch Dis Child. 2012;97:533-8.
Lietman SA, Germain-Lee EL, Levine MA. Hypercalcemia in children and adolescents. Curr Opin Pediatr. 2010;22:508-15.
Babar G, Alemzadeh R. A case of acute psychosis in an adolescent male. Case Rep Endocrinol. 2014;2014:937631.
Bai M, Pearce SH, Kifor O, Trivedi S, Stauffer UG, Thakker RV, et al. In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium homeostasis as a cause of secondary hyperparathyroidism in familial benign hypocalciuric hypercalcemia. J Clin Invest. 1997;99:88-96.
Bushinsky DA, Monk RD. Electrolyte quintet: Calcium. Lancet. 1998;352:306-11.
Demir K, Döneray H, Kara C, Atay Z, Çetinkaya S, Çayır A, et al. Comparison of treatment regimens in management of severe hypercalcemia due to vitamin D ıntoxication in children. J Clin Res Pediatr Endocrinol. 2019;11:140-8.
Çullas İlarslan NE, Şıklar Z, Berberoğlu M. Childhood sustained hypercalcemia: a diagnostic challenge. J Clin Res Pediatr Endocrinol. 2017;9:315-22.
Kollars J, Zarroug AE, van Heerden J, Lteif A, Stavlo P, Suarez L, et al. Primary hyperparathyroidism in pediatric patients. Pediatrics. 2005;115:974-80.
Roizen J, Levine MA. Primary hyperparathyroidism in children and adolescents. J Chin Med Assoc. 2012;75:425-34.
Markowitz ME, Underland L, Gensure R. Parathyroid Disorders. Pediatr Rev. 2016;37:524-35.
Shafiei B, Hoseinzadeh S, Fotouhi F, Malek H, Azizi F, Jahed A, et al. Preoperative 99 mTc-sestamibi scintigraphy in patients with primary hyperparathyroidism and concomitant nodular goiter: comparison of SPECT-CT, SPECT, and planar imaging. Nucl Med Commun. 2012;33:1070-6.
Li L, Chen L, Yang Y, Han J, Wu S, Bao Y, et al. Giant anterior mediastinal parathyroid adenoma. Clin Nucl Med. 2012;37:889-91.
Mostoufi-Moab S, Ward LM. Skeletal morbidity in children and adolescents during and following cancer therapy. Horm Res Paediatr. 2019;91:137-51.
McKay C, Furman WL. Hypercalcemia complicating childhood malignancies. Cancer. 1993;72:256-60.
Inukai T, Hirose K, Inaba T, Kurosawa H, Hama A, Inada H, et al. Hypercalcemia in childhood acute lymphoblastic leukemia: frequent implication of parathyroid hormone-related peptide and E2A-HLF from translocation 17;19. Leukemia. 2007;21:288-96.
Castellano E, Attanasio R, Boriano A, Pellegrino M, Borretta G. Serum phosphate: a neglected test in the clinical management of primary hyperparathyroidism. J Clin Endocrinol Metab. 2022;107:e612-8.
Düğer H, Bostan H, Gül Ü, Uçan B, Hepşen S, Sakız D, et al. The importance of hypophosphatemia in the clinical management of primary hyperparathyroidism. J Endocrinol Invest. 2023;46:1935-40.
Isik G, Bozdag PG. Why is childhood urolithiasis increasing? Etiology, diagnosis and management: a single-center experience. J Nephrol. 2023;36:1599-604.
Harman CR, van Heerden JA, Farley DR, Grant CS, Thompson GB, Curlee K. Sporadic primary hyperparathyroidism in young patients: a separate disease entity? Arch Surg. 1999;134:651-5.
Kızılcan Çetin S, Şıklar Z, Aycan Z, Özsu E, Ceran A, Erisen Karaca S, et al. clinical profile of parathyroid adenoma in children and adolescents: a single-center experience. Turk Arch Pediatr. 2023;58:56-61.
Rampp RD, Mancilla EE, Adzick NS, Levine MA, Kelz RR, Fraker DL, et al. Single gland, ectopic location: adenomas are common causes of primary hyperparathyroidism in children and adolescents. World J Surg. 2020;44:1518-25.
Hsu SC, Levine MA. Primary hyperparathyroidism in children and adolescents: the Johns Hopkins Children’s Center experience 1984-2001. J Bone Miner Res. 2002;17 Suppl 2:N44-50.
Sakao Y, Sugiura T, Tsuji T, Ohashi N, Yasuda H, Fujigaki Y, et al. Clinical manifestation of hypercalcemia caused by adrenal insufficiency in hemodialysis patients: a case-series study. Intern Med. 2014;53:1485-90.
Schoelwer MJ, Viswanathan V, Wilson A, Nailescu C, Imel EA. Infants with congenital adrenal hyperplasia are at risk for hypercalcemia, hypercalciuria, and nephrocalcinosis. J Endocr Soc. 2017;1:1160-7.
Madihi Y, Mostofizadeh N, Shamsipour Dehkordi H, Riahinezhad M, Hovsepian S, Rostampour N, et al. Prevalence of nephrocalcinosis in children with congenital adrenal hyperplasia. J Res Med Sci. 2022;27:16.
Babar GS, Tariq M. Challenges of diagnosing pseudohypoaldosteronism (PHA) in an infant. Case Rep Endocrinol. 2022;2022:9921003.
Vaidya A, Brown JM, Williams JS. The renin-angiotensin-aldosterone system and calcium-regulatory hormones. J Hum Hypertens. 2015;29:515-21.
Demirbilek H, Alanay Y, Alikaşifoğlu A, Topçu M, Mornet E, Gönç N, et al. Hypophosphatasia presenting with pyridoxine-responsive seizures, hypercalcemia, and pseudotumor cerebri: case report. J Clin Res Pediatr Endocrinol. 2012;4:34-8.
Christensen SE, Nissen PH, Vestergaard P, Mosekilde L. Familial hypocalciuric hypercalcaemia: a review. Curr Opin Endocrinol Diabetes Obes. 2011;18:359-70.
Koca SB. Cinacalcet therapy in a child with novel homozygous CASR p.Glu353Lys mutation causing familial hypocalciuric hypercalcemia type 1: case report and review of the literature. Turk J Pediatr. 2023;65:853-61.
Phitayakorn R, McHenry CR. Hyperparathyroid crisis: use of bisphosphonates as a bridge to parathyroidectomy. J Am Coll Surg. 2008;206:1106-15.
Alagaratnam S, Kurzawinski TR. Aetiology, diagnosis and surgical treatment of primary hyperparathyroidism in children: new trends. Horm Res Paediatr. 2015.


