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1.
Pediatr Nephrol ; 39(3): 799-806, 2024 Mar.
Article in English | MEDLINE | ID: mdl-37733097

ABSTRACT

BACKGROUND: Nutcracker syndrome (NCS) describes a set of symptoms and signs resulting from compression of the left renal vein (LRV). There is a lack of knowledge about its natural course, diagnosis, and management, especially in children. Herein, we present our single-center experience with a large number of patients who have long-term follow-up results. METHODS: All patients with NCS diagnosed between January 2011 and March 2021 were included and their data were obtained retrospectively. RESULTS: A total of 123 NCS patients (85 females) were included. The median age at the time of diagnosis was 12 (IQR 10-14) years, and BMI percentiles were below 5% in 38% of the cases. At the time of diagnosis, two-thirds of the patients were asymptomatic. The most common laboratory finding was nephritic proteinuria (98%), followed by microscopic hematuria (16%). Signs of LRV compression were significantly more evident in upright position Doppler ultrasonography (DUS) examination. All patients have been followed conservatively; hematuria and/or proteinuria resolved in 43 of the 108 patients (40%) within 35.8 ± 25.8 months of follow-up. Control DUS was performed in 52 patients after a mean period of 39.1 ± 21.3 months. The median peak velocity and diameter ratios of the LRV in the upright position were found to be decreased significantly when compared to the initial assessment (p < 0.05). Normal DUS findings were noted in 13 patients at the final evaluation. CONCLUSIONS: In unexplained proteinuria and/or hematuria, NCS should be considered, especially in asthenic adolescents. Our results support conservative management in children as the first-line treatment approach.


Subject(s)
Hematuria , Renal Nutcracker Syndrome , Female , Adolescent , Humans , Child , Follow-Up Studies , Hematuria/diagnosis , Hematuria/etiology , Retrospective Studies , Ultrasonography , Renal Nutcracker Syndrome/diagnosis , Renal Nutcracker Syndrome/diagnostic imaging , Renal Veins/diagnostic imaging , Proteinuria/diagnosis , Proteinuria/etiology , Proteinuria/therapy
2.
Postgrad Med ; 135(6): 588-592, 2023 Aug.
Article in English | MEDLINE | ID: mdl-37309906

ABSTRACT

OBJECTIVES: Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory disease. Recurrent fever, serositis, and arthritis are common findings of the disease. In addition, musculoskeletal complaints such as exertional leg pain can be overlooked, although they are common and affect patients' quality of life. The aim of this study was to evaluate the frequency of exertional leg pain in pediatric FMF patients and to analyze the association of this finding with other characteristics of FMF. METHODS: The files of FMF patients were retrospectively evaluated. The clinical characteristics and disease severity of the patients with exertional leg pain were compared with the patients without exertional leg pain. International severity scoring system for FMF (ISSF) and Mor severity score were used for assessment. RESULTS: The study included 541 FMF patients (287 females), 149 (27.5%) with exertional leg pain. The median colchicine dosage was significantly higher in patients with exertional leg pain (p = 0.02), arthritis (p = 0.001) and arthralgia (p˂0.001) were encountered more frequently in the attacks of these patients. The median disease severity scores calculated by both Mor severity scale and ISSF were significantly higher in patients with exertional leg pain compared to those without (p˂0.001). In the group of patients with exertional leg pain, the M694V mutation, either in one allele or in two alleles, was found to be significantly more common (p = 0.006 and p˂0.001, respectively). CONCLUSIONS: Exertional leg pain in pediatric FMF patients is the component of moderate-to-severe disease course, and this may be considerably associated with the presence of M694V mutation.


Subject(s)
Arthritis , Familial Mediterranean Fever , Female , Humans , Familial Mediterranean Fever/complications , Familial Mediterranean Fever/genetics , Retrospective Studies , Leg , Quality of Life , Phenotype , Arthralgia/genetics , Arthralgia/complications , Mutation
3.
Clin Pediatr (Phila) ; 62(6): 548-550, 2023 06.
Article in English | MEDLINE | ID: mdl-36457163

ABSTRACT

A male newborn was investigated for history of antenatal hyperechogenic colon (HEC) detected at 32 weeks of gestation. In the first week of life, urinary ultrasonography showed nephrolithiasis. Urinary amino acid analysis expressed increased excretion of dibasic amino acids, and high urinary cystine levels were detected in both spot and 24-hour urine specimens. He was diagnosed as cystinuria, and genetic analysis of the patient revealed a heterozygous mutation in SLC7A9 gene. Antenatal presentation of cystinuria with HEC is rare and reported to be associated with a more severe disease course.


Subject(s)
Cystinuria , Infant, Newborn , Male , Humans , Female , Pregnancy , Cystinuria/diagnostic imaging , Cystinuria/genetics , Cystinuria/metabolism , Mutation , Colon/diagnostic imaging
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