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ALKAPTONURIA – A CASE REPORT

Ana Parlov
Marin Petrić
Dijana Perković
Dušanka Martinović Kaliterna

Puni tekst: hrvatski, pdf (386 KB) str. 0-0 preuzimanja: 96* citiraj
APA 6th Edition
Parlov, A., Petrić, M., Perković, D. i Martinović Kaliterna, D. (2017). ALKAPTONURIJA – PRIKAZ BOLESNICE. Liječnički vjesnik, 139 (7-8), 0-0. Preuzeto s https://hrcak.srce.hr/189781
MLA 8th Edition
Parlov, Ana, et al. "ALKAPTONURIJA – PRIKAZ BOLESNICE." Liječnički vjesnik, vol. 139, br. 7-8, 2017, str. 0-0. https://hrcak.srce.hr/189781. Citirano 21.07.2019.
Chicago 17th Edition
Parlov, Ana, Marin Petrić, Dijana Perković i Dušanka Martinović Kaliterna. "ALKAPTONURIJA – PRIKAZ BOLESNICE." Liječnički vjesnik 139, br. 7-8 (2017): 0-0. https://hrcak.srce.hr/189781
Harvard
Parlov, A., et al. (2017). 'ALKAPTONURIJA – PRIKAZ BOLESNICE', Liječnički vjesnik, 139(7-8), str. 0-0. Preuzeto s: https://hrcak.srce.hr/189781 (Datum pristupa: 21.07.2019.)
Vancouver
Parlov A, Petrić M, Perković D, Martinović Kaliterna D. ALKAPTONURIJA – PRIKAZ BOLESNICE. Liječnički vjesnik [Internet]. 2017 [pristupljeno 21.07.2019.];139(7-8):0-0. Dostupno na: https://hrcak.srce.hr/189781
IEEE
A. Parlov, M. Petrić, D. Perković i D. Martinović Kaliterna, "ALKAPTONURIJA – PRIKAZ BOLESNICE", Liječnički vjesnik, vol.139, br. 7-8, str. 0-0, 2017. [Online]. Dostupno na: https://hrcak.srce.hr/189781. [Citirano: 21.07.2019.]

Sažetak
A 63-year-old patient, who was for a long time suspicious of inflammatory rheumatic disease (seronegative rheumatoid arthritis, spondyloarthropathies), was hospitalized due to progression of pain in the hips, knees and small joints of the hand. A few years ago she noticed that her ears and tip of the nose were flooded and urine was tarnishing in air. These symptoms fit the clinical presentation of an inherited metabolic disease alkaptonuria. Our patient manifested with arthropathy and also with the ochronosis (bluish black pigmentation of nails, scleras, cartilages, joints). The suspicion of alkaptonuria was confirmed by the analysis of urine in which elevated levels of the homogentisic acid were found. The purpose of this paper is to present a rare disease that mimics the inflammatory rheumatic diseases and degenerative changes in the joints, and for which there has not yet been discovered a specific treatment.

Ključne riječi
Alkaptonuria – complications, diagnosis; Ochronosis – complications, diagnosis, etiology; Homogentisic acid – metabolism, urine; Spondylarthropathies – etiology; Arthritis, rheumatoid – etiology; Pigmentation disorders – etiology

Hrčak ID: 189781

URI
https://hrcak.srce.hr/189781

[hrvatski]

Posjeta: 322 *