Medullary sponge kidney - the mysterious name of a simple disease

Medullary sponge kidney (renal spongiosis), (MSK) is a rare developmental anomaly of the kidney of unknown cause. It is presumed, that people with a genetic predisposition (<5% family occurrence) are prone to the disease. The peak of diagnosis is between the ages of 20-50, usually by chance (due...
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Autor*in:	Karol Bigosiński [verfasserIn] Maciej Dubaj [verfasserIn] Aleksandra Dembowska [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch ; Spanisch ; Polnisch ; Russisch ; Ukrainisch

Erschienen:	2022

Schlagwörter:	kidneys medullary sponge kidney calcification kidney failure

Übergeordnetes Werk:	In: Journal of Education, Health and Sport - Kazimierz Wielki University, 2017, 12(2022), 8
Übergeordnetes Werk:	volume:12 ; year:2022 ; number:8

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.12775/JEHS.2022.12.08.058

Katalog-ID:	DOAJ036227161

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callnumber-first	G - Geography, Anthropology, Recreation
author	Karol Bigosiński
spellingShingle	Karol Bigosiński misc GV557-1198.995 misc kidneys misc medullary sponge kidney misc calcification misc kidney failure misc Education misc L misc Sports misc Medicine misc R Medullary sponge kidney - the mysterious name of a simple disease
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topic_title	GV557-1198.995 Medullary sponge kidney - the mysterious name of a simple disease kidneys medullary sponge kidney calcification kidney failure
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title	Medullary sponge kidney - the mysterious name of a simple disease
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title_full	Medullary sponge kidney - the mysterious name of a simple disease
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title_sort	medullary sponge kidney - the mysterious name of a simple disease
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title_auth	Medullary sponge kidney - the mysterious name of a simple disease
abstract	Medullary sponge kidney (renal spongiosis), (MSK) is a rare developmental anomaly of the kidney of unknown cause. It is presumed, that people with a genetic predisposition (<5% family occurrence) are prone to the disease. The peak of diagnosis is between the ages of 20-50, usually by chance (due to lack of symptoms) during an abdominal X-ray, where the so-called nephrocalcinosis (calcifications in the kidney) can be observed. Another radiologic test, that may suggest the condition in question is abdominal ultrasound, where cysts up to 8 mm in diameter in the medullary part of the kidney and calcifications can be seen. Diagnosis may also be based on the diagnosis of pre-existing stones and urinary tract infections, or hematuria. Urography has the highest sensitivity to sponge kidney. Symptoms, if already present, are characterized by low back pain, hematuria, hematuria, recurrent urinary tract infections, proteinuria, sterile purulence. Ultimately, the aforementioned pathologies can lead to kidney failure. To date, no causal treatment has been developed; only symptomatic treatment of lithiasis foci and urinary tract infections is possible. The purpose of the following paper was to describe the definition, epidemiology and etiology of MSK and to highlight the randomness of diagnosis and the problem in the lack of specific therapy for this renal developmental disorder. Current publications and guidelines from scientific societies around the world were reviewed, using MeSH-compliant keywords.
abstractGer	Medullary sponge kidney (renal spongiosis), (MSK) is a rare developmental anomaly of the kidney of unknown cause. It is presumed, that people with a genetic predisposition (<5% family occurrence) are prone to the disease. The peak of diagnosis is between the ages of 20-50, usually by chance (due to lack of symptoms) during an abdominal X-ray, where the so-called nephrocalcinosis (calcifications in the kidney) can be observed. Another radiologic test, that may suggest the condition in question is abdominal ultrasound, where cysts up to 8 mm in diameter in the medullary part of the kidney and calcifications can be seen. Diagnosis may also be based on the diagnosis of pre-existing stones and urinary tract infections, or hematuria. Urography has the highest sensitivity to sponge kidney. Symptoms, if already present, are characterized by low back pain, hematuria, hematuria, recurrent urinary tract infections, proteinuria, sterile purulence. Ultimately, the aforementioned pathologies can lead to kidney failure. To date, no causal treatment has been developed; only symptomatic treatment of lithiasis foci and urinary tract infections is possible. The purpose of the following paper was to describe the definition, epidemiology and etiology of MSK and to highlight the randomness of diagnosis and the problem in the lack of specific therapy for this renal developmental disorder. Current publications and guidelines from scientific societies around the world were reviewed, using MeSH-compliant keywords.
abstract_unstemmed	Medullary sponge kidney (renal spongiosis), (MSK) is a rare developmental anomaly of the kidney of unknown cause. It is presumed, that people with a genetic predisposition (<5% family occurrence) are prone to the disease. The peak of diagnosis is between the ages of 20-50, usually by chance (due to lack of symptoms) during an abdominal X-ray, where the so-called nephrocalcinosis (calcifications in the kidney) can be observed. Another radiologic test, that may suggest the condition in question is abdominal ultrasound, where cysts up to 8 mm in diameter in the medullary part of the kidney and calcifications can be seen. Diagnosis may also be based on the diagnosis of pre-existing stones and urinary tract infections, or hematuria. Urography has the highest sensitivity to sponge kidney. Symptoms, if already present, are characterized by low back pain, hematuria, hematuria, recurrent urinary tract infections, proteinuria, sterile purulence. Ultimately, the aforementioned pathologies can lead to kidney failure. To date, no causal treatment has been developed; only symptomatic treatment of lithiasis foci and urinary tract infections is possible. The purpose of the following paper was to describe the definition, epidemiology and etiology of MSK and to highlight the randomness of diagnosis and the problem in the lack of specific therapy for this renal developmental disorder. Current publications and guidelines from scientific societies around the world were reviewed, using MeSH-compliant keywords.
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title_short	Medullary sponge kidney - the mysterious name of a simple disease
url	https://doi.org/10.12775/JEHS.2022.12.08.058 https://doaj.org/article/4c374daaab5242debbbf4b9974645fb9 https://apcz.umk.pl/JEHS/article/view/39403 https://doaj.org/toc/2391-8306
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code="u">https://doi.org/10.12775/JEHS.2022.12.08.058</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doaj.org/article/4c374daaab5242debbbf4b9974645fb9</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://apcz.umk.pl/JEHS/article/view/39403</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/2391-8306</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_DOAJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield 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Medullary sponge kidney - the mysterious name of a simple disease

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