ABSTRACT
BACKGROUND: Eosinophilic peritonitis is a relatively rare entity. Kimura's disease is a rare chronic inflammatory disorder of unknown etiology, characterized by subcutaneous nodules mainly in the head and neck region, regional lymphadenopathy and occasional involvement of kidney. There is currently no report of eosinophilic peritonitis in Kimura's disease. CASE PRESENTATION: A 44-year-old Chinese man presented with abdominal distention, nausea, vomiting and edema in lower limbs for 1 month. Laboratory data showed elevated eosinophils in peripheral blood and ascites, nephrotic syndrome with progressively renal dysfunction, and elevated IgE. Ultrasonography of lymph nodes showed multiple lymphadenopathy in bilateral inguinal regions. Surgical excision was performed for one of the enlarged lymph nodes and histopathology revealed diagnosis of Kimura's disease. Renal biopsy indicated focal segmental glomerulosclerosis (FSGS) and acute tubulointerstitial nephritis with infiltration of eosinophils in renal interstitium. The patient was prescribed with oral prednisolone therapy (30 mg/day), and underwent continuous ambulatory peritoneal dialysis (CAPD). The peripheral and peritoneal eosinophil count decreased rapidly and normalized within 2 days. Forty-five days after prednisolone therapy, partial remission of nephrotic syndrome and decrease of serum creatinine were achieved while peritoneal dialysis dosage had decreased. Inguinal lymph nodes gradually shrunk in size. The overall conditions remain stable afterwards. CONCLUSIONS: This rare case highlighted the clinical conundrum of a patient presenting with eosinophilic peritonitis, lymphadenopathy, nephrotic syndrome and renal failure associated with Kimura's disease. The remarkable eosinophilia, pathology of lymph node and kidney, as well as significant response to steroids should guide towards the diagnosis.
Subject(s)
Glomerulosclerosis, Focal Segmental/pathology , Kimura Disease , Nephritis, Interstitial/pathology , Nephrotic Syndrome , Peritoneal Dialysis, Continuous Ambulatory/methods , Prednisolone/administration & dosage , Adult , Biopsy/methods , Eosinophilia/diagnosis , Eosinophilia/etiology , Glucocorticoids/administration & dosage , Humans , Kidney Function Tests/methods , Kimura Disease/blood , Kimura Disease/diagnosis , Kimura Disease/physiopathology , Lymphadenopathy/etiology , Lymphadenopathy/pathology , Male , Nephrotic Syndrome/etiology , Nephrotic Syndrome/pathology , Nephrotic Syndrome/physiopathology , Nephrotic Syndrome/therapy , Peritonitis/diagnosis , Peritonitis/etiology , Treatment Outcome , Ultrasonography/methodsSubject(s)
Abdominal Cavity/diagnostic imaging , Endoscopy, Gastrointestinal/methods , Eosinophilia , Immunoglobulin E/blood , Intestine, Small , Kimura Disease , Abdominal Pain/diagnosis , Diagnosis, Differential , Eosinophilia/diagnosis , Eosinophilia/etiology , Glomerulonephritis, Membranous/pathology , Humans , Intestine, Small/diagnostic imaging , Intestine, Small/pathology , Kimura Disease/blood , Kimura Disease/diagnosis , Kimura Disease/physiopathology , Male , Middle Aged , Tomography, X-Ray Computed/methodsSubject(s)
Kimura Disease/physiopathology , Adult , Age Factors , China , Female , Humans , Kimura Disease/pathology , Male , Young AdultABSTRACT
BACKGROUND: Kimura's disease (KD) is known to be dominant among young Asian men, but it can also occur in middle- and advanced-aged people. The clinical characteristics of KD, especially by age, are not well known. AIM: This study was performed to investigate the effects of age on the clinical characteristics of KD. DESIGN: We conducted a case series study. METHODS: All case studies of patients diagnosed with KD were collected via a PubMed search of studies published until August 2018. The data were analyzed by age group. RESULTS: In total, 215 studies were reviewed (238 patients; mean age of 36 years). The male:female ratio was 4:1 overall, 17:1 in patients aged <20 years, 4:1 in patients aged 20-39 years and 2:1 in patients aged ≥40 years (P = 0.01). The percentage of patients with pruritus was 15.4% overall, 3.8% in patients aged <20 years, 15.5% in patients aged 20-39 years and 21.7% in patients aged ≥40 years (P = 0.02). The time to diagnosis was 5.3 years overall, 3.2 years in patients aged <20 years, 4.7 years in patients aged 20-39 years and 7.1 years in patients aged ≥40 years (P < 0.01). CONCLUSIONS: The proportion of female patients affected the incidence of pruritus, and the time to diagnosis increased as the patients' age increased. There were no significant age-related differences in region/race, complications, multiplicity, laterality, anatomical distribution, maximum size, eosinophil count, immunoglobulin E level, initial treatment, recurrence or outcomes. This may be useful information for the diagnosis of KD.
