• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제25권4호
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• pp.293-299
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• 2022

Purpose: Data on eosinophilic esophagitis (EoE) in South America is scarce. Moreover, no studies are available in Ecuador. We evaluated the clinical, endoscopic, and histological characteristics of Ecuadorian children with EoE. Methods: Medical records of 2,711 children who underwent upper gastrointestinal endoscopy (UGE) between 2009 and 2020 at Hospital Metropolitano de Quito, Ecuador were reviewed. Esophageal mucosal biopsies were obtained from 72 patients and the features of 35 children with EoE were described. EoE was diagnosed when there were more than 15 eosinophils in the esophagus, per high power field. Results: EoE was diagnosed in 35 children (9.4±4.5 years) with a male predominance (74%). Abdominal pain (51.4%) and vomiting (31.4%) were dominant symptoms. A history of allergic diseases was noted in 47.1% of the children, which mainly included allergic rhinitis (37.1%) and atopic dermatitis (11.4%). The most common endoscopic findings were furrowing (82.9%) and edema (74.3%). All patients were initially treated with proton-pump inhibitors (PPIs). Those who did not respond to PPIs received steroids (5.7%) and diet therapy (5.7%), and five patients were referred to an allergist. Clinical and histological resolution was observed in 65% of the patients who underwent a second UGE after 6-8 weeks of PPI. Conclusion: Our study describes the clinical features of pediatric EoE in Ecuador. This is the first retrospective study in Ecuador that describes the clinical, endoscopic, and histological manifestations of EoE in a small pediatric population. Almost half of the children who underwent a biopsy had EoE.

• Journal of Digestive Cancer Research
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• 제5권2호
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• pp.120-124
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• 2017

A-49-year-old male patient with no specific medical history was admitted to the clinic because of persistent epigastric pain radiating to back for 4 months. He had multiple parenchymal tumors in body and tail of pancreas, para-spinal muscle, and mediastinum on abdomen CT image. Cytologic examination of the pancreas which was done by endoscopic ultrasound guided fine needle aspiration (EUS-FNA) showed adenocarcinoma, whereas histological examination of the para-spinal mass showed undifferentiated sarcoma. Histologic examination of the pancreatic mass was made through endoscopic ultrasound guided fine needle biopsy (EUS-FNB) for accurate diagnosis, and the histologic examination of both the pancreas and posterior mediastinal mass showed the same undifferentiated sarcoma. Therefore, we reviewed the cytopathic tissue obtained from the pancreas for the first time, and it was confirmed to be similar to histologic findings in the mediastinal mass.

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제19권1호
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• pp.71-75
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• 2016

Esophageal candidiasis is commonly seen in immunocompromised patients; however, candida esophagitis induced stricture is a very rare complication. We report the first case of esophageal stricture secondary to candidiasis in a glycogen storage disease (GSD) 1b child. The patient was diagnosed with GSD type 1b by liver biopsy. No mutation was found in the G6PC gene, but SLC37A4 gene sequencing revealed a compound heterozygous mutation (p.R28H and p.W107X, which was a novel mutation). The patient's absolute neutrophil count was continuously under $1,000/{\mu}L$ when he was over 6 years of age. He was admitted frequently for recurrent fever and infection, and frequently received intravenous antibiotics, antifungal agents. He complained of persistent dysphagia beginning at age 7 years. Esophageal stricture and multiple whitish patches were observed by endoscopy and endoscopic biopsy revealed numerous fungal hyphae consistent with candida esophagitis. He received esophageal balloon dilatation four times, and his symptoms improved.

• 대한두경부종양학회지
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• 제24권1호
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• pp.69-72
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• 2008

Lymphomas of the nasal sinuses are relatively uncommon and represent less than 1% of all head and neck malignancies. Most common symptoms are nasal obstruction, epistaxis, rhinorrhea. We report a case of primary extranodal diffuse large B-cell non-Hodgkin's lymphoma in nasal sinuses accompanying with exophthalmos. A 70-year-old male patient was referred to our hospital with exophthalmos and severe septal deviation. We conducted endoscopic biopsy with septoplasty and biopsy result was diffuse large B-cell lymphoma. He received chemotherapy(R-CHOP) and radiotherapy. At follow-up, he remained free of disease.

• 대한두경부종양학회지
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• 제32권2호
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• pp.19-22
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• 2016

Adenosquamous carcinoma (ASC) of the larynx is very rare malignancy which has well defined two distinctive pathological features, an adenocarcinoma and a squamous cell carcinoma (SCC). Diagnosis of ASC by endoscopic biopsy is challenging due to small amount of harvested tissue. ASC has a worse prognosis than SCC with an early lymph node metastasis and a distant dissemination. We experienced a rare case of vocal fold ASC which was initially misdiagnosed as atypical squamous cell proliferation at frozen biopsy. We reported this case with a literature review.

• 대한상부위장관⦁헬리코박터학회지
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• 제18권3호
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• pp.209-212
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• 2018

We report a rare case of systemic amyloidosis with gastrointestinal and lymph node involvement. A 64-year-old woman was admitted to our hospital with dyspepsia and weight loss. Initial esophagogastroduodenoscopy (EGD) revealed nonspecific findings, and abdominal computed tomography showed necrotizing lymphadenopathy at the porta hepatis. Laparoscopic lymph node biopsy was performed under suspicion of tuberculous lymphadenopathy, but a definite diagnosis was not established. Follow-up EGD performed 6 months later revealed multiple telangiectasia-like lesions at the gastric body, and endoscopic biopsy revealed amyloid deposition. Through additional blood and urine protein electrophoresis, the patient was finally diagnosed with systemic amyloidosis associated with multiple myeloma. She was treated with dexamethasone, thalidomide, and bortezomib; however, she died 3 months after diagnosis because of pneumonia and multiple organ failure.

• Clinical and Experimental Pediatrics
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• 제49권3호
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• pp.268-272
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• 2006

목 적 : Helicobacter pylori 재감염률은 내시경적 생검만이 가능했던 시대에는 $^{13}C$-요소 호기 검사의 출현 이후에 비해 높게 보고되었다. 소아는 일반적으로 침습적인 내시경적 생검을 시행하기 용이치 않다. 본 연구는 $^{13}C$-요소 호기 검사와 내시경적 생검에 의한 재감염률을 비교하고, 그 차이에 영향을 미치는 인자를 찾고자 하였다. 방 법 : H. pylori 감염으로 치료받고 박멸이 확인된 소아들을 대상으로 하였다. 박멸 확인 후 18개월이 경과한 시점에 재감염을 확인하기 위하여 내시경적 생검(n=34명, 평균 연령 $11.5{\pm}3.7$세) 혹은 $^{13}C$-요소 호기 검사를(n=38명, 평균 연령 $10.0{\pm}3.6$세) 시행하였다. 첫 진단 시 내시경적 생검으로 위전정부 및 체부에서 세 절편을 채취하여 urease 검사, Giemsa 염색 및 Warthin-Starry 염색이 모두 양성으로 나오거나 생검 조직에서 H. pylori균이 배양된 경우 감염된 것으로 판정하였고, 박멸 치료 1-3개월 후 모든 검사상 음성인 경우 박멸된 것으로 판정하였다. $^{13}C$-요소 호기 검사는 최소 4시간 금식 후 75 mg의 $^{13}C$-요소를 주스에 섞어 마시도록 하는데, 복용 전 및 30분 후 Helikit(Isodiagnostika, Alberta, Canada)를 이용하여 숨을 불어넣도록 하고 delta $^{13}C$ per mil이 4.00 이상일 때를 양성으로 판독하였다. 결 과 : 내시경적 생검을 시행하였을 때 재감염률은 35.3%(12/34)였다. 내시경적 생검을 받은 모두가 당시 복부 증상이 있어 $^{13}C$-요소 호기 검사를 시행한 경우에 비해 복부 증상이 있는 경우가 유의하게 많았다(P=0.000). $^{13}C$-요소 호기 검사를 시행하였을 때 재감염률은 13.2%(5/38)였다. 추적 관찰 시 복부 증상이 있는 경우 재감염률이 유의하게 높았으며(P=0.008), 성별(P=0.694), 연령별(P=0.827). 궤양과 비궤양 간(P=0.730), 치료 방법 간에는(P=0.087) 재감염률에 차이를 보이지 않았다. 결 론 : 한국 소아에서 H. pylori 박멸 후 18개월이 경과하였을 때 비침습적인 $^{13}C$-요소 호기 검사를 이용한 재감염률은 13.2%이다. 내시경적 생검은 정확하나 침습적이어서 특히 무증상인 소아의 경우 이를 기피할 확률이 높아, 순응도에 따라 많은 영향을 받는다. 소아에서 재감염률 조사를 평가할 때에는 비침습적이면서 간편한 방법인가를 고려하여야 할 것이다.

• Tuberculosis and Respiratory Diseases
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• 제56권4호
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• pp.374-380
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• 2004

목 적 : 폐암의 진단에 있어서 진단율이 낮은 기관지주위나 점막하 병변에서 TBNA의 진단율을 조직 생검과 비교하여 TBNA의 임상적인 유용성에 대해 조사하였다. 방 법 : 연세대학교 의과대학 세브란스병원에서 1994년 1월부터 2002년 12월까지 5,582예의 굴곡성 기관지내시경검사를 시행하였으며, 기관지주위나 점막하 병변을 보여 TBNA와 조직생검을 시행한 환자 중 폐암이 확진되었던 120예를 대상으로 후향적으로 조사하였다. 결 과 : 기관지주위나 점막하 병변을 가진 폐암에서 TBNA의 진단율은 75.8%로 생검(52.5%)에 비해 진단율이 높았으며(p=0.001), 생검 단독에 비해 TBNA와 생검을 병용하는 경우 진단율이 유의하게 높았다(88.3%, p=0.0001). 폐암의 세포형이나 내시경적 형태에 따른 TBNA의 진단율은 유의한 차이가 없었으나, 소세포암에서 좀 더 높았다. 결 론 : 기관지주위나 점막하 병변을 가진 폐암의 진단에 있어서 TBNA는 생검보다 진단율이 높았고 생검과 같이 시행함으로써 폐암의 진단율을 향상시킬 수 있었다.

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제26권1호
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• pp.50-57
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• 2023

Purpose: The purpose of this study was to determine the pattern of human leukocyte antigen (HLA)-DQ genotype in children diagnosed with celiac disease (CD) (biopsy proven), and to compare this with a control group; and secondarily, to correlate HLA genotypes with clinical profiles of CD. Methods: This cross-sectional comparative observational study included 26 controls and 52 patients diagnosed with CD who presented at Sir Padampat Mother and Child Health Institute, Jaipur, from May, 2017 to October, 2018. HLA DQ genotype was assessed for each patients and correlated with clinical profiles. Results: HLA DQ2/DQ8 genotypes were significantly more common in CD (present in 100.0% cases) than in controls (23.1%) in Northern India (Rajasthan). When HLA DQ2.5 and DQ8 were present together, individuals had significantly more atypical presentations and severe findings on duodenal biopsy. Similarly, patients with the HLA DQ 2.5 genotype were also predisposed to more severe endoscopic findings, while HLA DQ2.2 predisposed them to less severe biopsy findings. HLA DQ8 was significantly associated with later age at diagnosis (>5 years) and shorter stature. The highest HLA DQ relative risk (RR) for CD development was associated with HLA DQ2.5 and DQ2.2 in combination, followed by HLA DQ2.5 and DQ8 in combination, while HLA DQx.5 and HLA DQ2.2 together had the lowest risk. Conclusion: HLA DQ2/DQ8 genotypes are strongly associated with pediatric CD patients in northern India. These genotypes and their combinations may be associated with different clinical presentations of CD, and may help predict severity of CD.

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제14권2호
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• pp.122-129
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• 2011

The persistence of jaundice beyond the first 2 weeks of life require further investigation and this can be determined if the conjugated bilirubin levels are greater than 1.5 mg/dL or greater than 20% of the total bilirubin level. There is a diverse differential diagnosis for the cause of neonatal cholestasis due to hepatobiliary disease including biliary atresia, which eventually leads to liver cirrhosis if uncorrected before 60~80 days of life. Long-established initial studies include abdominal ultrasonography, hepatobiliary scintigraphy and liver biopsy, but better diagnostic methods are needed. Promising new options are described including MRCP (magnetic resonance cholangiography), ERCP (endoscopic retrograde cholangiography), and PCC (percutaneous cholecysto-cholangiography). Though no single test can differentiate biliary atresia from other neonatal cholestasis with confidence, a combination of diagnostic methods is usually consistently beneficial. By excluding biliary atresia as early as possible, the risk of unnecessary explolaparotomy with intraoperative cholangiography is decreased. Further evaluation would be required for the diagnosis of neonatal cholestasis after excluding biliary atresia.