Case Reports in Gastrointestinal Medicine最新文献

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Less is More: Nasogastric Tube Perforation in a Patient With Prior Roux-en-Y Gastric Bypass. 少即是多:先前Roux-en-Y胃旁路术患者的鼻胃管穿孔。
IF 0.5
Case Reports in Gastrointestinal Medicine Pub Date : 2025-12-17 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/2949430
Mario Tavakoli, Sam Papasotiriou, Dustin R Fraidenburg
{"title":"Less is More: Nasogastric Tube Perforation in a Patient With Prior Roux-en-Y Gastric Bypass.","authors":"Mario Tavakoli, Sam Papasotiriou, Dustin R Fraidenburg","doi":"10.1155/crgm/2949430","DOIUrl":"10.1155/crgm/2949430","url":null,"abstract":"<p><p>Nasogastric (NG) tube placement is a routine inpatient procedure that is generally considered safe. NG perforation is a rare complication, but when it occurs, it is often serious or even deadly. The risk for perforation is increased in patients with a history of connective tissue disorders, inflammatory bowel disease, or prior abdominal surgeries such as Roux-en-Y gastric bypass (RYB). We present a fatal case of a 51-year-old woman with a recent RYB who suffered an NG-tube perforation leading to peritonitis and septic shock. This case highlights the extreme care healthcare providers must have when placing NG tubes in patients with prior abdominal surgeries, while offering suggestions on how to minimize the risk of fatal complications.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"2949430"},"PeriodicalIF":0.5,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12714115/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145805810","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mesenteric Venous Malformation With Subocclusive Symptoms: A Case Report. 肠系膜静脉畸形伴亚封闭症状1例报告
IF 0.5
Case Reports in Gastrointestinal Medicine Pub Date : 2025-11-29 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/8396838
Joseph Amara, Elio Mikhael, Santa El Helou, Jad Hachem, Rita Slim, César Yaghi
{"title":"Mesenteric Venous Malformation With Subocclusive Symptoms: A Case Report.","authors":"Joseph Amara, Elio Mikhael, Santa El Helou, Jad Hachem, Rita Slim, César Yaghi","doi":"10.1155/crgm/8396838","DOIUrl":"10.1155/crgm/8396838","url":null,"abstract":"<p><p>Venous malformations, previously referred to as cavernous hemangiomas, can affect the gastrointestinal tract and rarely the mesentery. When symptomatic, it can cause pain, hematochezia, or less frequently obstructive symptoms. In this paper, we report the case of a 60-year-old man who presented to the emergency department for abdominal pain and subocclusive symptoms. A CT scan with intravenous contrast revealed a well-defined mesenteric mass measuring 3.5 × 3.2 cm in the pelvic region with a localized anterior panniculitis. A surgical resection was performed which led to resolution of obstructive symptoms, with the histopathological analysis confirming the diagnosis of mesenteric venous malformation.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"8396838"},"PeriodicalIF":0.5,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12681416/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145702137","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acute Pancreatitis After Initiating Dulaglutide in a Patient Previously Treated With a DPP-4 Inhibitor: Case Report From Palestine. 先前接受DPP-4抑制剂治疗的患者在使用杜拉鲁肽后出现急性胰腺炎:来自巴勒斯坦的病例报告。
IF 0.5
Case Reports in Gastrointestinal Medicine Pub Date : 2025-11-28 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/9918202
Alisse Nasser, Hosniyeh Ladadweh, Raed Madia, Ahmad Dalashi, Adnan Wahdan, Abdullah Alawi
{"title":"Acute Pancreatitis After Initiating Dulaglutide in a Patient Previously Treated With a DPP-4 Inhibitor: Case Report From Palestine.","authors":"Alisse Nasser, Hosniyeh Ladadweh, Raed Madia, Ahmad Dalashi, Adnan Wahdan, Abdullah Alawi","doi":"10.1155/crgm/9918202","DOIUrl":"10.1155/crgm/9918202","url":null,"abstract":"<p><strong>Background: </strong>Dulaglutide, a glucagon-like peptide-1 (GLP-1) agonist, is utilized for the management of type 2 diabetes and obesity, typically administered subcutaneously at a dosage of 0.75 mg/0.5 mL once weekly, with adjustments made as needed. While typically well tolerated, it may induce infrequent yet severe adverse effects, including acute pancreatitis.</p><p><strong>Case presentation: </strong>In this case report, we present the first documented case of GLP-1-induced pancreatitis in Palestine. A 62-year-old female Palestinian patient with a history of type 2 diabetes complicated with nephropathy, hypertension, dyslipidemia, and cardiac catheterization three years prior without stenting. The patient developed acute pancreatitis following the initiation of 1.5 mg of a GLP-1 receptor agonist after 4 months of therapy. The patient experienced upper abdominal pain radiating to the back, nausea, and alternating diarrhea and constipation for 5 days. Laboratory investigations revealed elevated serum amylase and lipase levels, and imaging studies confirmed signs of acute pancreatitis. After the GLP-1 agonist was discontinued, the patient's symptoms improved, and she fully recovered.</p><p><strong>Conclusion: </strong>GLP-1 receptor agonists are advantageous for the management of diabetes and obesity but may precipitate acute pancreatitis in predisposed individuals. Clinicians should be aware of this potential risk and promptly investigate any patient who presents with signs of acute abdominal pain during GLP-1 therapy.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"9918202"},"PeriodicalIF":0.5,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12680473/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145701991","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Septic Shock and Multiorgan Failure Related to Liver Abscess Caused by Fish Bone Penetration of Duodenal Wall. 鱼骨穿透十二指肠壁致肝脓肿脓毒性休克及多器官功能衰竭。
IF 0.5
Case Reports in Gastrointestinal Medicine Pub Date : 2025-11-12 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/8462610
Md Atiquzzaman, Injamam Ull Haque, Md Motiul Islam, Tarikul Hamid, Mohammad Rabiul Halim, Kazi Nuruddin Ahmed, Sadia Jesmin, Rajib Hasan, Quazi Abdullah Al Masum, Md Ashikuzzaman Sohan
{"title":"Septic Shock and Multiorgan Failure Related to Liver Abscess Caused by Fish Bone Penetration of Duodenal Wall.","authors":"Md Atiquzzaman, Injamam Ull Haque, Md Motiul Islam, Tarikul Hamid, Mohammad Rabiul Halim, Kazi Nuruddin Ahmed, Sadia Jesmin, Rajib Hasan, Quazi Abdullah Al Masum, Md Ashikuzzaman Sohan","doi":"10.1155/crgm/8462610","DOIUrl":"10.1155/crgm/8462610","url":null,"abstract":"<p><p>We report an intriguing case of an 80-year-old male presented with high-grade fever and severe upper abdominal pain. An abdominal ultrasound indicated a deep-seated abscess in the Segment IV of liver. An elusive diagnosis was made after Contrast Enhanced Computed Tomography (CECT) scan of whole abdomen which disclosed a sharp, pointed fish bone accommodating between the distal part of gastric antrum and cavitary lesion of liver. In the operative room, an upper GI endoscopy revealed a healed duodenal ulcer. An explorative laparotomy was performed subsequently, and the perihepatic abscess cavity was drained along with the removal of fish bone about 3.15 cm in length from perihilar region without any damage to the adjoining structures. His management was centered around IV antibiotics, imaging, and subsequent surgical drainage. The gentleman made a good recovery.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"8462610"},"PeriodicalIF":0.5,"publicationDate":"2025-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12629700/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145565687","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
When Gas Replaces the Liver: A Rare Case of Successfully Treated Emphysematous Hepatitis. 当气代替肝:一例成功治疗的肺气性肝炎。
IF 0.5
Case Reports in Gastrointestinal Medicine Pub Date : 2025-11-11 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/5558002
Dirin Ukwade, Hasan S Raza, Omar T Ahmed, James S Love, Maria El Gemayel, Jamie L Berkes
{"title":"When Gas Replaces the Liver: A Rare Case of Successfully Treated Emphysematous Hepatitis.","authors":"Dirin Ukwade, Hasan S Raza, Omar T Ahmed, James S Love, Maria El Gemayel, Jamie L Berkes","doi":"10.1155/crgm/5558002","DOIUrl":"10.1155/crgm/5558002","url":null,"abstract":"<p><p>Emphysematous hepatitis is a rare condition characterized by the presence of gas within the hepatic parenchyma. Only a limited number of cases have been reported, with most patients experiencing poor outcomes and median survival time ranging from hours to days after diagnosis. We present a case of a patient with uncontrolled diabetes, abdominal pain, and fatigue who was found to have emphysematous hepatitis. The patient was successfully treated with antibiotics and percutaneous drainage without the need for surgical intervention. This case represents the second reported instance of survival following percutaneous drainage, highlighting the potential efficacy of this minimally invasive approach.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"5558002"},"PeriodicalIF":0.5,"publicationDate":"2025-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12626690/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145558070","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tapeworm-Induced Eosinophilic Colitis: A Case Report. 绦虫诱导嗜酸性结肠炎1例。
IF 0.5
Case Reports in Gastrointestinal Medicine Pub Date : 2025-11-07 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/8743086
Mujaheed Suleman, Jay Lodhia, Marianne Gnanamuttupulle, Alex Mremi, Omar Said, Felister Uisso, Ayesiga Herman
{"title":"Tapeworm-Induced Eosinophilic Colitis: A Case Report.","authors":"Mujaheed Suleman, Jay Lodhia, Marianne Gnanamuttupulle, Alex Mremi, Omar Said, Felister Uisso, Ayesiga Herman","doi":"10.1155/crgm/8743086","DOIUrl":"10.1155/crgm/8743086","url":null,"abstract":"<p><p>Eosinophilic colitis is a rare gastrointestinal (GI) pathology characterised by abnormal eosinophilic infiltration into the digestive tract's mucosa. It can present as a primary disorder or as a secondary manifestation, with a wide range of clinical presentations, necessitating a broad differential diagnosis by clinicians. We report an unusual case of eosinophilic colitis caused by a tapeworm in a young male who presented with intestinal obstruction. This case underscores the diagnostic challenges associated with eosinophilic colitis and highlights the essential role of histopathology in confirming the diagnosis. The absence of standardised histological criteria for eosinophil counts in colonic mucosa further complicates the diagnosis. Consequently, management should be individualised, taking into account the patient's condition and the underlying aetiology.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"8743086"},"PeriodicalIF":0.5,"publicationDate":"2025-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12618116/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145543243","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Drug-Induced Liver Failure Following Topical Minoxidil: A Case Report. 局部米诺地尔引起的药物性肝衰竭1例报告。
IF 0.5
Case Reports in Gastrointestinal Medicine Pub Date : 2025-11-04 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/1040092
Katrin Premke, Matthias Kästner, Carlos Fritzsche, Andreas Erbersdobler, Micha Loebermann
{"title":"Drug-Induced Liver Failure Following Topical Minoxidil: A Case Report.","authors":"Katrin Premke, Matthias Kästner, Carlos Fritzsche, Andreas Erbersdobler, Micha Loebermann","doi":"10.1155/crgm/1040092","DOIUrl":"10.1155/crgm/1040092","url":null,"abstract":"<p><strong>Introduction: </strong>Drug-induced liver failure (DILI) is one of the causes of acute liver injury (13%-20%), encompassing both predictable and idiosyncratic reactions. While the latter are rare, it can lead to severe liver damage in vulnerable patients. Although topical minoxidil is a widely used treatment for androgenetic alopecia, cases of liver failure linked to its use are extremely uncommon and have not been widely described. This case report discusses the potential for severe liver injury following topical minoxidil application.</p><p><strong>Case presentation: </strong>A 21-year-old female with no significant medical history presented with jaundice, elevated liver enzymes, and impaired liver function three and a half weeks after starting topical minoxidil for alopecia areata. Laboratory tests revealed significantly elevated transaminases, bilirubin, and disturbed coagulation. A liver biopsy revealed centrilobular necrosis, which indicated drug-induced liver damage. After discontinuation of minoxidil, the patient's condition improved rapidly, with a marked decrease in liver enzymes and disappearance of clinical symptoms.</p><p><strong>Conclusions: </strong>This is the first evidence of severe drug-induced liver failure associated with topical minoxidil. It underscores the potential for hepatotoxicity even with over-the-counter drugs that are thought to have minimal systemic absorption. The rapid improvement after discontinuation of the drug and exclusion of differential diagnoses suggests a causal relationship. In cases of severe liver failure of unclear origin, all substances should be considered in the case history.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"1040092"},"PeriodicalIF":0.5,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12614736/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145543283","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Endoscopic Ultrasound With Fine Needle Biopsy Confirming a Diagnosis of Immune Checkpoint Inhibitor-Related Type 3 Autoimmune Pancreatitis. 内镜超声加细针活检证实免疫检查点抑制相关的3型自身免疫性胰腺炎的诊断。
IF 0.5
Case Reports in Gastrointestinal Medicine Pub Date : 2025-10-31 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/5519015
Dana Ley, Kusum Sharma, Saqib Walayat, Mark R Albertini, Rashmi M Agni, Deepak V Gopal
{"title":"Endoscopic Ultrasound With Fine Needle Biopsy Confirming a Diagnosis of Immune Checkpoint Inhibitor-Related Type 3 Autoimmune Pancreatitis.","authors":"Dana Ley, Kusum Sharma, Saqib Walayat, Mark R Albertini, Rashmi M Agni, Deepak V Gopal","doi":"10.1155/crgm/5519015","DOIUrl":"10.1155/crgm/5519015","url":null,"abstract":"<p><strong>Introduction: </strong>Immune checkpoint inhibitor-related pancreatitis, also known as type 3 autoimmune pancreatitis (AIP), is uncommon and has a widely ranging clinical presentation. We present the biopsy findings of a case consistent with type 3 AIP-an entity recently described in the literature, the pathologic findings of which have not been well characterized.</p><p><strong>Case report: </strong>A 71-year-old male with metastatic mucosal melanoma of the urethra was treated with immune checkpoint inhibitor (ICI) therapy (nivolumab/relatlimab) and developed vague epigastric discomfort. He was found to have an elevated lipase, which increased to > 20x the upper limit of normal. Subsequent imaging showed new infiltrative masses in the pancreatic head and distal body/tail. Endoscopic ultrasound with fine needle biopsy (FNB) was performed. This showed T-lymphocyte predominant infiltrates, in the acini and septal areas, with concomitant acinar, duct, and venular damage, including both CD4 and CD8 lymphocytes, which were considered consistent with type 3 AIP. He was treated successfully with prednisone.</p><p><strong>Discussion: </strong>On biopsy, there was no evidence of malignancy or features of type 1 or type 2 AIP. Histologic findings included moderate infiltration and damage to the pancreatic parenchyma, ductal, and vascular structures by CD4 and CD8 lymphocytes, pointing to immune-mediated pancreatic injury, and supportive of ICI-mediated injury to the pancreas of this patient. The clinical presentation of type 3 AIP ranges from asymptomatic lipase elevation to asymptomatic pancreatitis to acute symptomatic pancreatitis. There may be no clear temporal relationship to treatment initiation. Type 3 AIP typically presents along with other immune-related adverse events. Endoscopic ultrasound with FNB contributed to diagnostic certainty in this case and changed our patient's management, allowing for appropriate treatment of his immune-related adverse event.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"5519015"},"PeriodicalIF":0.5,"publicationDate":"2025-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12595219/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145483373","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Atypical Presentation of Colonic Sarcoidosis and Current Diagnostic Challenges. 结肠结节病的不典型表现和当前的诊断挑战。
IF 0.5
Case Reports in Gastrointestinal Medicine Pub Date : 2025-10-31 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/5549338
Rangesh Modi, Cameron Dandridge, Nada Attia, Edwin McDonald
{"title":"Atypical Presentation of Colonic Sarcoidosis and Current Diagnostic Challenges.","authors":"Rangesh Modi, Cameron Dandridge, Nada Attia, Edwin McDonald","doi":"10.1155/crgm/5549338","DOIUrl":"10.1155/crgm/5549338","url":null,"abstract":"<p><p>We present a case of a Hispanic woman in her 70s who presented with nonspecific lower abdominal pain leading to a diagnosis of hepatic and colonic sarcoidosis. She had elevated liver function tests (LFTs), and imaging ruled out ischemia and cholangitis but revealed a cecal and ascending colon wall thickening with fat stranding. Infectious and autoimmune causes of elevated LFTs were excluded. A liver biopsy showed noncaseating granulomas, indicating hepatic sarcoidosis. Despite no bloody diarrhea, a colonoscopy was performed due to nonspecific abdominal pain and imaging-based evidence of colitis. A colonoscopy revealed diffuse areas of severely erythematous, hyperemic, and ulcerating mucosa in the ascending colon. Biopsies confirmed abundant noncaseating granulomas in the background of inflammation. Stool testing, imaging, and staining of biopsies excluded infectious or ischemic etiologies of colitis. The presence of hepatic sarcoidosis, along with age and symptom profile, prompted a diagnosis of colonic sarcoidosis rather than Crohn's colitis. Prednisone and methotrexate improved her symptoms and LFTs within 3 months of initiation.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"5549338"},"PeriodicalIF":0.5,"publicationDate":"2025-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12595241/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145483315","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Simultaneous Presentation of Post-Transplant Lymphoproliferative Disorder (PTLD) and Acute Cellular Rejection (ACR) in a Liver Transplant Recipient: A Therapeutic Conundrum. 肝移植受者同时出现移植后淋巴增生性疾病(PTLD)和急性细胞排斥反应(ACR):一个治疗难题。
IF 0.5
Case Reports in Gastrointestinal Medicine Pub Date : 2025-10-29 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/1627234
Ankit Mishra, Matthew Kubina, Dhiraj K Peddu, Benjamin L Viglianti, Anamarija M Perry, Priya Kathuria, Hellan Kwon, Shannon A Carty, Patricia Bloom
{"title":"Simultaneous Presentation of Post-Transplant Lymphoproliferative Disorder (PTLD) and Acute Cellular Rejection (ACR) in a Liver Transplant Recipient: A Therapeutic Conundrum.","authors":"Ankit Mishra, Matthew Kubina, Dhiraj K Peddu, Benjamin L Viglianti, Anamarija M Perry, Priya Kathuria, Hellan Kwon, Shannon A Carty, Patricia Bloom","doi":"10.1155/crgm/1627234","DOIUrl":"10.1155/crgm/1627234","url":null,"abstract":"<p><p>We report a 64-year-old liver transplant recipient who developed early nondestructive post-transplant lymphoproliferative disorder (PTLD) and severe acute cellular rejection (ACR) concurrently. Hepatic lymphadenopathy led to a liver biopsy demonstrating early PTLD. Immunosuppression (IS) was reduced for early PTLD, which led to acute liver injury requiring high-dose steroids. However, subsequent augmentation in immunosuppression for ACR led to progression of PTLD, requiring rituximab treatment. This case highlights the complexity of managing conflicting liver transplant complications and underscores the importance of a multidisciplinary approach. In our case, prioritizing the treatment of rejection preserved the allograft function. Long-term follow-up showed complete resolution of both rejection and PTLD.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"1627234"},"PeriodicalIF":0.5,"publicationDate":"2025-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12588761/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145460197","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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