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The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome

Cilt: 10 Sayı: 2 25 Haziran 2020
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The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome

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INTRODUCTION: Creatinine was started to be used as a marker of glomerular filtration rate (GFR) in 1920’s. Later in the 1990s, cystatin C was shown to be superior to creatinine in assessing GFR. In some patients, glomerular filtration of cystatin C was found to be low compared to creatinine, and it was hypothesized that glomerular pores may have been shrunken in these patients. For the group of patients having a cystatin C based estimation of GFR (eGFR cystatin C) to creatinine-based estimation of GFR (eGFR creatinine) ratio of ≤60%, the pathophysiological classification is defined as Shrunken Pore Syndrome.

CASE: A 16-month-old female patient was admitted to Ege University Pediatric nephrology clinic with the diagnosis of neurogenic bladder secondary to meningomyelocele. She had a history of antenatal meningomyelocele, and hydrocephalus diagnosed as Arnold Chiari type 2. On postnatal day 1, she had undergone meningomyelocele sac excision and ventriculoperitoneal shunt operation. There was no history of pyelonephritis. Systemic examination revealed a dysmorphic facial appearance, operation scar on her back and syndactyly of the toes, and paraplegia on neurological examination. In laboratory examination; urea: 24 mg/dL, creatinine: 0.3 mg/dL, parathormone: 47 ng/mL, cystatin C: 1.4 mg/L (RR: 0.53-0.95), blood β2 microglobulin: 2716 ng/mL. Patient’s eGFRcystatin C: 107 ml/min/1.73m2 and eGFRcreatinine: 188 ml/min/1.73m2. Shrunken Pore Syndrome was considered due to the difference between the patient's eGFRcystatin C value and eGFRcreatinine value.

CONCLUSION: Shrunken Pore Syndrome has no known treatment; however, it is important to diagnose these patients because of accompanying risks such as increased cardiac mortality. With the usage of cystatin C as a marker of GFR, possible mortality risks can be predictable and preventive measures can be taken early on.

Anahtar Kelimeler

Kaynakça

  1. [1] Kyhse-Andersen J, Schmidt C, Nordin G, Andersson B, Nilsson-Ehle P, Lindström V, Grubb A. Serum cystatin C, determined by a rapid, automated particle-enhanced turbidimetric method, is a better marker than serum creatinine for glomerular filtration rate. Clin Chem 1994;40:1921–6.
  2. [2] Christensson A, Grubb A, Molvin J, Holm H, Gransbo K, Tasevska-Dinevska G, Bachus E, Jujic A, Magnusson M. The shrunken pore syndrome is associated with declined right ventricular systolic function in a heart failure population - the HARVEST study. Scand J Clin Lab Invest. 2016; 76:568-74.
  3. [3] Purde MT, Nock S, Risch L, Medina Escobar P, Grebhardt C, Nydegger UE, Stanga Z, Risch M. The cystatin C/creatinine ratio, a marker of glomerular filtration quality: associated factors, reference intervals, and prediction of morbidity and mortality in healthy seniors. Transl Res 2016;169:80–90.
  4. [4] Grubb A, Lindström V, Jonsson M, Bäck SE, Åhlund T, Rippe B, Christensson A. Reduction in glomerular pore size is not restricted to pregnant women. Evidence for a new syndrome: “Shrunken pore syndrome”. Scand J Clin Lab Invest 2015;75:333–40.
  5. [5] Emil den Bakker, Reinoud Jbj Gemke, Joanna Ae van Wijk, Isabelle Hubeek, Birgit Stoffel-Wagner & Arend Bökenkamp (2019): Evidence for shrunken pore syndrome in children, Scandinavian Journal of Clinical and Laboratory Investigation, DOI: 10.1080/00365513.2019.1692231
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Ayrıntılar

Birincil Dil

İngilizce

Konular

Sağlık Kurumları Yönetimi

Bölüm

Olgu Sunumu

Yayımlanma Tarihi

25 Haziran 2020

Gönderilme Tarihi

12 Mart 2020

Kabul Tarihi

26 Nisan 2020

Yayımlandığı Sayı

Yıl 2020 Cilt: 10 Sayı: 2

Kaynak Göster

APA
Taner, S., İşdaş, B., Kaplan Bulut, İ., Conkar, S., & Kabasakal, C. (2020). The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome. Journal of Contemporary Medicine, 10(2), 284-286. https://izlik.org/JA77EJ84ZU
AMA
1.Taner S, İşdaş B, Kaplan Bulut İ, Conkar S, Kabasakal C. The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome. Journal of Contemporary Medicine. 2020;10(2):284-286. https://izlik.org/JA77EJ84ZU
Chicago
Taner, Sevgin, Başak İşdaş, İpek Kaplan Bulut, Seçil Conkar, ve Caner Kabasakal. 2020. “The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome”. Journal of Contemporary Medicine 10 (2): 284-86. https://izlik.org/JA77EJ84ZU.
EndNote
Taner S, İşdaş B, Kaplan Bulut İ, Conkar S, Kabasakal C (01 Haziran 2020) The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome. Journal of Contemporary Medicine 10 2 284–286.
IEEE
[1]S. Taner, B. İşdaş, İ. Kaplan Bulut, S. Conkar, ve C. Kabasakal, “The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome”, Journal of Contemporary Medicine, c. 10, sy 2, ss. 284–286, Haz. 2020, [çevrimiçi]. Erişim adresi: https://izlik.org/JA77EJ84ZU
ISNAD
Taner, Sevgin - İşdaş, Başak - Kaplan Bulut, İpek - Conkar, Seçil - Kabasakal, Caner. “The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome”. Journal of Contemporary Medicine 10/2 (01 Haziran 2020): 284-286. https://izlik.org/JA77EJ84ZU.
JAMA
1.Taner S, İşdaş B, Kaplan Bulut İ, Conkar S, Kabasakal C. The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome. Journal of Contemporary Medicine. 2020;10:284–286.
MLA
Taner, Sevgin, vd. “The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome”. Journal of Contemporary Medicine, c. 10, sy 2, Haziran 2020, ss. 284-6, https://izlik.org/JA77EJ84ZU.
Vancouver
1.Sevgin Taner, Başak İşdaş, İpek Kaplan Bulut, Seçil Conkar, Caner Kabasakal. The Pediatric Case of a Recently Defined Syndrome: Shrunken Pore Syndrome. Journal of Contemporary Medicine [Internet]. 01 Haziran 2020;10(2):284-6. Erişim adresi: https://izlik.org/JA77EJ84ZU