Amyloidosis is a rare disease that results from the deposition of extracellular protein in various body tissues, causing progressive organ dysfunction. Secondary renal amyloidosis is a rare but serious complication of chronic inflammatory bowel disease, particularly in patients with Crohn’s disease or ulcerative colitis. We report a case of secondary renal amyloidosis in a pediatric patient who reported a 16-year history of “very early onset inflammatory bowel disease”. Intensive treatment including repeated infliximab infusions improved clinical parameters of inflammatory bowel disease, although renal dysfunction showed progression. Amyloidosis should be considered in patients with IBD, particularly if they suffered disease progression.
Amyloidosis is a clinical disorder caused by the deposition of an extracellular insoluble protein in various body tissues, which causes progressive organ dysfunction. Amyloidosis can be classified into primary or secondary types, and the deposition of amyloid fibrils can be localized or systemic [
Secondary amyloidosis predominantly affects the kidneys, and renal involvement is the most important predictor of survival in patients. Clinical manifestations of renal amyloidosis include proteinuria, nephrotic syndrome, renal insufficiency and progression to end-stage renal failure [
We report a pediatric case of IBD complicated with renal amyloidosis. This study was approved by the Seoul National University Hospital's Institutional Review Board (IRB No. 1808-130-967).
A 19-year-old young man with a long-term history of IBD was referred to the Division of Nephrology, Department of Pediatrics, Seoul National University Children’s Hospital, Seoul, Korea with a high serum creatinine level (1.55 mg/dL). The patient reported history of rectal bleeding at 3 years old age, and he was tentatively diagnosed with an anal fissure and constipation. A year later, he developed bloodtinged stool and abdominal pain. Clinical, laboratory, and colonoscopic examinations at our hospital led to a diagnosis of colonic angiodysplasia and iron deficiency anemia. He was managed with blood transfusion and iron supplementation. A year thereafter, he developed bilateral knee joint pain with swelling and tested positive for the perinuclear anti-neutrophil cytoplasmic antibody. Colonoscopic examination showed severe colitis throughout the colon, and a colonic biopsy revealed chronic active colitis without granuloma formation. He was diagnosed with ulcerative colitis and treated with oral azathioprine, mesalazine, and prednisolone for 5 years. At 10 years of age, his family moved to their home-town, and he was followed-up at a local hospital and received only mesalazine. At 15 years of age, he was admitted to that hospital with new-onset abdominal pain and vomiting. Abdominal computed tomography revealed a segmental polypoid mass at the sigmoid colon, and he was referred to our hospital for further evaluation of the mass. At our hospital, he underwent total proctocolectomy with ileal pouch-anal anastomosis. Histopathological examination of the mass revealed stage II moderately differentiated sigmoid colon cancer. Postoperatively, he experienced persistent abdominal pain with diarrhea and weight loss over the subsequent 6 months. Follow-up gastrointestinal endoscopy revealed features of Crohn’s disease involving the upper gastrointestinal tract, as well as the small bowel and the colon. Granulomas were detected in all 7 biopsy specimens examined. He was treated with intravenous methylprednisolone and oral azathioprine followed by 18 infusions of infliximab (200 mg/dose) administered every 6 weeks, which led to improvement in his gastrointestinal symptoms and inflammatory parameters. Thereafter, he was lost to follow-up for 2 years. At 18 years of age, he was admitted to another hospital with acute abdominal pain. He was treated with 3 infusions of infliximab followed by 12 infusions of adalimumab over 9 months followed by the administration of oral corticosteroid and azathioprine. However, he was re-referred to our hospital owing to persistent diarrhea with severe abdominal pain. Infliximab infusion was re-initiated concomitant with oral azathioprine and rifaximin. A month later, he was referred to the Division of Nephrology owing to new-onset azotemia. He was 153 cm tall (<3rd percentile) and weighed 37.4 kg (<3rd percentile). Physical examination was unremarkable except for his poor general condition. Laboratory tests revealed his hemoglobin was 9.1 g/dL, serum creatinine level was 1.55 mg/dL, estimated glomerular filtration rate (eGFR) calculated using the Schwartz formula was 40.6 mL/min/1.73m2, serum albumin level was 2.7 g/dL, and C-reactive protein was 9.9 mg/dL. Serological tests including serum complement C3 and C4, anti-nuclear antibody, antineutrophil cytoplasmic antibody, and anti-double stranded DNA were all negative. Urinalysis showed 3+ proteinuria and microscopic hematuria, and 24-hour urinary protein excretion was 5.9 g/day. Renal ultrasonography showed bilateral globular kidneys with increased renal parenchymal echogenicity and splenomegaly. Renal biopsy revealed deposits of amorphous pinkish material in the mesangial matrix and vascular walls (
Amyloidosis is a single- or multiorgan disease caused by the extracellular deposition of low-molecular weight, insoluble, rigid, and amorphous proteinaceous material. To date, 25 different proteins causing amyloidosis have been identified. The formation of amyloid commences with the misfolding of amyloidogenic precursor proteins followed by self-aggregation and the formation of protofilaments from the misfolded proteins. Amyloid fibrils comprise 4–6 protofilaments showing a β-pleated sheet configuration and produce birefringence under polarized light when stained using the Congo red dye. Amyloid deposition causes structural and functional impairment of the affected tissues and organs [
Amyloidosis can be classified on the basis of: 1) the nature of the precursor proteins or, 2) the distribution of amyloid deposits. Localized amyloidosis involves the local production and deposition of an amyloidogenic protein (commonly immunoglobulin light chains) within the affected organ. Systemic amyloidosis involves the deposition of circulating amyloidogenic proteins in various organs. Primary amyloidosis (amyloid light-chain [AL] amyloidosis), the most common type, is characterized by the deposition of excess immunoglobulin light chains in patients with multiple myeloma, lymphoma, or other lymphoproliferative diseases. Secondary amyloidosis (amyloid A [AA] amyloidosis) is caused by the deposition of N-terminal fragments of SAA proteins in patients with chronic inflammatory, infectious, or neoplastic diseases. SAA is an acute phase reactant protein, which is produced during sustained inflammatory conditions [
Secondary amyloidosis is a rare but serious complication of cancers, chronic infections, or chronic inflammatory disorders including IBD, particularly Crohn’s disease [
Diagnosis of renal amyloidosis is confirmed by histopathological examination showing amyloid deposition within tissues. Light microscopic examination using hematoxylin and eosin stains shows amorphous material within the mesangium and the glomerular capillary loops. The gold standard of diagnosis is Congo red staining of amyloid, showing apple-green birefringence under polarized light. Electron microscopic examination reveals non-branching amyloid fibrils [
Our patient reported a long-term history of IBD with a complicated disease course. The earlier part of the case with ulcerative colitis and sigmoid colon cancer was reported previously [
The Pediatric Modification of the Montreal Classification for IBD: The Paris Classification was proposed in 2011 [
While IBD primarily affects the gastrointestinal tract, extraintestinal manifestations occur in approximately 25 % of pediatric patients [
Secondary amyloidosis primarily affects the kidneys, and common clinical manifestations are proteinuria, nephrotic syndrome, and renal insufficiency. Proteinuria is more common than renal insufficiency at the time of diagnosis [
Early diagnosis of renal amyloidosis in patients with IBD may prevent further loss of organ function [
In conclusion, we report a case of secondary renal amyloidosis in a pediatric patient who reported a 16-year history of “very early onset inflammatory bowel disease”. Intensive treatment including repeated infliximab infusions improved clinical parameters of inflammatory bowel disease, although renal dysfunction showed progression. Amyloidosis should be considered in patients with IBD, particularly if they suffered disease progression.
This research was supported by a grant of the Korea Health Technology Research & Development Project through the Korea Health Industry Development Institute, funded by the Ministry of Health & Welfare, Republic of Korea (grant number: HI18C0013).
No potential conflict of interest relevant to this article was reported.
Image shows histopathological findings of a renal biopsy. (A) Deposition of amorphous pinkish material is observed in the glomeruli, blood vessels, and tubules (Periodic acid-Schiff stain, original magnification ×400). (B) Ultrastructurally, randomly arranged fine non-branching fibrils are observed in the glomeruli and the perivascular area (scale bar=1 μm). (C) Immunohistochemical examination shows diffusely and strongly stained amyloid A deposits in the glomeruli, blood vessels, and the tubules (original magnification ×400).