Pub Date : 2026-03-15eCollection Date: 2026-03-01DOI: 10.7759/cureus.105256
Pitchaya Jaruvijitrattana, Weeratian Tawanwongsri
Introduction Adult exfoliative dermatitis (ED) is a severe inflammatory dermatosis with heterogeneous etiologies and substantial morbidity. Hospital-based prospective data remain limited in Thailand. We aimed to prospectively describe the clinical characteristics, etiologies, management, and outcomes of adults with ED at a tertiary-care hospital in Thailand, and to assess changes during follow-up. Methods We conducted a prospective hospital-based cohort study enrolling consecutive adults diagnosed with ED from November 2024 to March 2026. Baseline demographics, comorbidities, prior treatments, clinical manifestations, and disease severity were recorded. Etiology was determined by clinicopathologic correlation and treating-physician adjudication. Patients were followed longitudinally for up to 12 months after diagnosis, and changes in disease severity and clinical outcomes were assessed during follow-up. Analyses were primarily descriptive. Exploratory comparisons across follow-up visits were reported using nonparametric tests with corresponding p-values. Results Thirty-four patients were recruited; two were lost to follow-up, and one had incomplete baseline data, leaving 31 for analysis. The mean age was 58.0 ± 18.2 years, and 74.2% were male. Most were managed as outpatients (67.7%), while 32.3% required hospitalization. Pruritus, scaling, and erythema were present in all patients. Nail involvement was frequent (64.5%), whereas pustules and mucosal involvement were uncommon (6.5% each). Systemic features occurred in a subset, including arthritis (25.8%), fever (16.1%), edema (16.1%), and lymphadenopathy (6.5%). Conclusions In this prospective hospital-based cohort, adult ED demonstrated uniform core cutaneous features with variable systemic involvement and a substantial proportion requiring hospitalization. These findings provide pragmatic clinical profiles to support early recognition and structured evaluation of etiology and complications in routine practice.
{"title":"Clinical Characteristics, Etiologies, Management, and Outcomes of Adult Exfoliative Dermatitis at Chao Phraya Abhaibhubejhr Hospital, Thailand: A Prospective Cohort Study.","authors":"Pitchaya Jaruvijitrattana, Weeratian Tawanwongsri","doi":"10.7759/cureus.105256","DOIUrl":"https://doi.org/10.7759/cureus.105256","url":null,"abstract":"<p><p>Introduction Adult exfoliative dermatitis (ED) is a severe inflammatory dermatosis with heterogeneous etiologies and substantial morbidity. Hospital-based prospective data remain limited in Thailand. We aimed to prospectively describe the clinical characteristics, etiologies, management, and outcomes of adults with ED at a tertiary-care hospital in Thailand, and to assess changes during follow-up. Methods We conducted a prospective hospital-based cohort study enrolling consecutive adults diagnosed with ED from November 2024 to March 2026. Baseline demographics, comorbidities, prior treatments, clinical manifestations, and disease severity were recorded. Etiology was determined by clinicopathologic correlation and treating-physician adjudication. Patients were followed longitudinally for up to 12 months after diagnosis, and changes in disease severity and clinical outcomes were assessed during follow-up. Analyses were primarily descriptive. Exploratory comparisons across follow-up visits were reported using nonparametric tests with corresponding p-values. Results Thirty-four patients were recruited; two were lost to follow-up, and one had incomplete baseline data, leaving 31 for analysis. The mean age was 58.0 ± 18.2 years, and 74.2% were male. Most were managed as outpatients (67.7%), while 32.3% required hospitalization. Pruritus, scaling, and erythema were present in all patients. Nail involvement was frequent (64.5%), whereas pustules and mucosal involvement were uncommon (6.5% each). Systemic features occurred in a subset, including arthritis (25.8%), fever (16.1%), edema (16.1%), and lymphadenopathy (6.5%). Conclusions In this prospective hospital-based cohort, adult ED demonstrated uniform core cutaneous features with variable systemic involvement and a substantial proportion requiring hospitalization. These findings provide pragmatic clinical profiles to support early recognition and structured evaluation of etiology and complications in routine practice.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105256"},"PeriodicalIF":1.3,"publicationDate":"2026-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12989080/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147469954","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}
Pub Date : 2026-03-15eCollection Date: 2026-03-01DOI: 10.7759/cureus.105283
Amaar Aamery, Hashim Ba Wazir, Mohammad Salem Amer, Elsadig Elmukashfi A Omer
Small intestinal fungal overgrowth (SIFO) is defined by an abnormal proliferation of fungal organisms, most commonly Candida species, within the small intestine. Fungal infections, particularly candidiasis, are recognized causes of gastrointestinal (GI) symptoms, especially in patients with underlying conditions, such as malignancy or diabetes mellitus (DM), and in those exposed to immunosuppressive therapies, corticosteroids, or prolonged antibiotic use. SIFO is an underrecognized cause of GI symptoms, including bloating, diarrhea, and malabsorption. In rare cases, excessive fungal colonization can lead to mechanical bowel obstruction. This case report describes a patient with advanced retroviral infection who developed small bowel obstruction secondary to SIFO, underscoring the diagnostic challenges, therapeutic approaches, and the critical importance of early recognition and management.
{"title":"Small Intestinal Fungal Overgrowth Mimicking a Surgical Abdomen and Presenting as Bowel Obstruction: A Case Report and Literature Review.","authors":"Amaar Aamery, Hashim Ba Wazir, Mohammad Salem Amer, Elsadig Elmukashfi A Omer","doi":"10.7759/cureus.105283","DOIUrl":"https://doi.org/10.7759/cureus.105283","url":null,"abstract":"<p><p>Small intestinal fungal overgrowth (SIFO) is defined by an abnormal proliferation of fungal organisms, most commonly <i>Candida</i> species, within the small intestine. Fungal infections, particularly candidiasis, are recognized causes of gastrointestinal (GI) symptoms, especially in patients with underlying conditions, such as malignancy or diabetes mellitus (DM), and in those exposed to immunosuppressive therapies, corticosteroids, or prolonged antibiotic use. SIFO is an underrecognized cause of GI symptoms, including bloating, diarrhea, and malabsorption. In rare cases, excessive fungal colonization can lead to mechanical bowel obstruction. This case report describes a patient with advanced retroviral infection who developed small bowel obstruction secondary to SIFO, underscoring the diagnostic challenges, therapeutic approaches, and the critical importance of early recognition and management.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105283"},"PeriodicalIF":1.3,"publicationDate":"2026-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12993699/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147482883","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}
Pub Date : 2026-03-14eCollection Date: 2026-03-01DOI: 10.7759/cureus.105219
Suneha Shelke, Rusheeth R Thummalapally
Treatment-resistant depression (TRD) presents a complex clinical challenge, particularly when comorbid with substance use disorders (SUDs) or other compulsive behaviors. With up to a third of major depressive disorder (MDD) patients failing to respond to standard antidepressant therapies, there is growing interest in interventions such as esketamine, a glutamatergic N-methyl-D-aspartate (NMDA) receptor antagonist approved for TRD in 2019, as an intranasal therapy. While esketamine has demonstrated efficacy in alleviating depressive symptoms of TRD, emerging data also point towards its potential in addressing compulsive and addictive behaviors, particularly in patients whose depression and SUDs are deeply intertwined. This review aims to evaluate and synthesize the current literature on the use of esketamine in treating not only TRD, but specifically its application in patients suffering from comorbid substance use and addiction-related behaviors. We aim to clarify the therapeutic mechanisms, examine both human and animal data, and identify whether esketamine offers a dual-modality treatment approach that concurrently reduces depressive symptoms and addictive tendencies. Across peer-reviewed studies, including randomized control trials, cohort analyses, systematic reviews, and preclinical investigations, findings suggest that esketamine may reduce drug-seeking behavior, attenuate cravings, and improve outcomes when combined with behavioral interventions (such as mindfulness-based therapy). In rodent models, esketamine significantly inhibited cocaine-seeking after various abstinence conditions, and clinical data point to its potential role in treating alcohol misuse. In conclusion, esketamine holds potential as a dual-action therapeutic in patients with TRD and comorbid addiction; however, further large-scale studies are needed to explore its therapeutic magnitude, duration of benefit, safety, and effects on substance use-related outcomes.
难治性抑郁症(TRD)呈现出复杂的临床挑战,特别是当与物质使用障碍(sud)或其他强迫行为合并症时。由于多达三分之一的重度抑郁症(MDD)患者对标准抗抑郁药物治疗无效,人们对艾氯胺酮等干预措施越来越感兴趣,艾氯胺酮是2019年批准用于TRD的谷氨酸能n -甲基- d -天冬氨酸(NMDA)受体拮抗剂。虽然艾氯胺酮已证明在缓解TRD抑郁症状方面有效,但新出现的数据也表明,它在解决强迫和成瘾行为方面具有潜力,特别是在抑郁症和sud深深交织在一起的患者中。本综述旨在评价和综合目前关于使用艾氯胺酮治疗TRD的文献,特别是其在患有共病物质使用和成瘾相关行为的患者中的应用。我们的目的是澄清治疗机制,检查人类和动物数据,并确定艾氯胺酮是否提供双重治疗方法,同时减少抑郁症状和成瘾倾向。在同行评议的研究中,包括随机对照试验、队列分析、系统评价和临床前调查,结果表明,艾氯胺酮可以减少寻求药物的行为,减弱对药物的渴望,并在与行为干预(如正念治疗)相结合时改善结果。在啮齿动物模型中,艾氯胺酮在各种戒断条件下显著抑制可卡因寻求,临床数据表明其在治疗酒精滥用方面的潜在作用。总之,艾氯胺酮在TRD和共病成瘾患者中具有双重作用治疗的潜力;然而,需要进一步的大规模研究来探索其治疗效果、获益持续时间、安全性以及对物质使用相关结果的影响。
{"title":"Evaluation of Current Evidence on the Efficacy of Esketamine in Treating Substance-Use Disorders in Patients With Treatment-Resistant Depression (TRD): A Narrative Review.","authors":"Suneha Shelke, Rusheeth R Thummalapally","doi":"10.7759/cureus.105219","DOIUrl":"10.7759/cureus.105219","url":null,"abstract":"<p><p>Treatment-resistant depression (TRD) presents a complex clinical challenge, particularly when comorbid with substance use disorders (SUDs) or other compulsive behaviors. With up to a third of major depressive disorder (MDD) patients failing to respond to standard antidepressant therapies, there is growing interest in interventions such as esketamine, a glutamatergic N-methyl-D-aspartate (NMDA) receptor antagonist approved for TRD in 2019, as an intranasal therapy. While esketamine has demonstrated efficacy in alleviating depressive symptoms of TRD, emerging data also point towards its potential in addressing compulsive and addictive behaviors, particularly in patients whose depression and SUDs are deeply intertwined. This review aims to evaluate and synthesize the current literature on the use of esketamine in treating not only TRD, but specifically its application in patients suffering from comorbid substance use and addiction-related behaviors. We aim to clarify the therapeutic mechanisms, examine both human and animal data, and identify whether esketamine offers a dual-modality treatment approach that concurrently reduces depressive symptoms and addictive tendencies. Across peer-reviewed studies, including randomized control trials, cohort analyses, systematic reviews, and preclinical investigations, findings suggest that esketamine may reduce drug-seeking behavior, attenuate cravings, and improve outcomes when combined with behavioral interventions (such as mindfulness-based therapy). In rodent models, esketamine significantly inhibited cocaine-seeking after various abstinence conditions, and clinical data point to its potential role in treating alcohol misuse. In conclusion, esketamine holds potential as a dual-action therapeutic in patients with TRD and comorbid addiction; however, further large-scale studies are needed to explore its therapeutic magnitude, duration of benefit, safety, and effects on substance use-related outcomes.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105219"},"PeriodicalIF":1.3,"publicationDate":"2026-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12988702/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147464481","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}
Pub Date : 2026-03-14eCollection Date: 2026-03-01DOI: 10.7759/cureus.105213
Tharindu Ruwanpathiranage, Henry Olorunfemi, Satyanarayana V Sagi, Susan Varughese, Samson O Oyibo
Acute pancreatitis is a common cause of hospital admission; however, cases secondary to medication use are rare. We report a case of drug-induced mild acute pancreatitis in a 33-year-old female with type 2 diabetes mellitus. The patient presented with a one-day history of vomiting and lower chest and epigastric pain after five months of starting sitagliptin therapy. She was also taking the combined oral contraceptive pill. Clinical examination revealed epigastric tenderness and signs of dehydration. Laboratory findings showed elevated white cell count, C-reactive protein, and triglyceride levels. Although the serum amylase level was not clinically significant, a contrast-enhanced computed tomography performed 24 hours after the onset of symptoms demonstrated pancreatic inflammation and peri-pancreatic fluid consistent with acute pancreatitis. Common etiologies, including gallstones and alcohol, were excluded through imaging and history. The patient was managed conservatively with intravenous fluids for hydration and intravenous insulin for the severe hypertriglyceridemia and ketoacidosis. Sitagliptin was discontinued and replaced with gliclazide as opposed to metformin, which she was intolerant to. The combined oral contraceptive pill was continued. She demonstrated gradual improvement with normalization of inflammatory markers and triglyceride levels, achieving full recovery by day five. This case highlights the importance of considering sitagliptin and other medications, such as the combined oral contraceptive pill, as potential causes of acute pancreatitis and emphasizes the need for early recognition and prompt discontinuation of the offending agent to ensure optimal outcomes in patients.
{"title":"Acute Pancreatitis in a Young Patient With Type 2 Diabetes Mellitus Taking Sitagliptin and the Combined Oral Contraceptive Pill.","authors":"Tharindu Ruwanpathiranage, Henry Olorunfemi, Satyanarayana V Sagi, Susan Varughese, Samson O Oyibo","doi":"10.7759/cureus.105213","DOIUrl":"https://doi.org/10.7759/cureus.105213","url":null,"abstract":"<p><p>Acute pancreatitis is a common cause of hospital admission; however, cases secondary to medication use are rare. We report a case of drug-induced mild acute pancreatitis in a 33-year-old female with type 2 diabetes mellitus. The patient presented with a one-day history of vomiting and lower chest and epigastric pain after five months of starting sitagliptin therapy. She was also taking the combined oral contraceptive pill. Clinical examination revealed epigastric tenderness and signs of dehydration. Laboratory findings showed elevated white cell count, C-reactive protein, and triglyceride levels. Although the serum amylase level was not clinically significant, a contrast-enhanced computed tomography performed 24 hours after the onset of symptoms demonstrated pancreatic inflammation and peri-pancreatic fluid consistent with acute pancreatitis. Common etiologies, including gallstones and alcohol, were excluded through imaging and history. The patient was managed conservatively with intravenous fluids for hydration and intravenous insulin for the severe hypertriglyceridemia and ketoacidosis. Sitagliptin was discontinued and replaced with gliclazide as opposed to metformin, which she was intolerant to. The combined oral contraceptive pill was continued. She demonstrated gradual improvement with normalization of inflammatory markers and triglyceride levels, achieving full recovery by day five. This case highlights the importance of considering sitagliptin and other medications, such as the combined oral contraceptive pill, as potential causes of acute pancreatitis and emphasizes the need for early recognition and prompt discontinuation of the offending agent to ensure optimal outcomes in patients.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105213"},"PeriodicalIF":1.3,"publicationDate":"2026-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12991383/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147476835","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}
Pub Date : 2026-03-13eCollection Date: 2026-03-01DOI: 10.7759/cureus.105145
Raquel Borrego, André Soveral, Sandra André
Nodular pulmonary amyloidosis is a rare entity characterized by extracellular deposits of amyloid protein in the pulmonary parenchyma, usually with a benign prognosis and often asymptomatic. We report a case of a 61-year-old man with a prior diagnosis of Sjögren's syndrome who, during routine follow-up, was found to have multiple asymptomatic pulmonary nodules in the right lung, with uptake on positron emission tomography-computed tomography (PET CT) (SUVmax 2.11). Surgical resection was performed, and histological analysis revealed nodular deposits of amyloid protein with kappa light chain predominance, without evidence of systemic involvement. This case highlights the importance of considering nodular pulmonary amyloidosis in the differential diagnosis of pulmonary nodules in patients with Sjögren's syndrome, emphasizing the need for histological evaluation to avoid misdiagnosis and inappropriate treatment.
{"title":"Nodular Pulmonary Amyloidosis Associated With Sjögren's Syndrome.","authors":"Raquel Borrego, André Soveral, Sandra André","doi":"10.7759/cureus.105145","DOIUrl":"10.7759/cureus.105145","url":null,"abstract":"<p><p>Nodular pulmonary amyloidosis is a rare entity characterized by extracellular deposits of amyloid protein in the pulmonary parenchyma, usually with a benign prognosis and often asymptomatic. We report a case of a 61-year-old man with a prior diagnosis of Sjögren's syndrome who, during routine follow-up, was found to have multiple asymptomatic pulmonary nodules in the right lung, with uptake on positron emission tomography-computed tomography (PET CT) (SUVmax 2.11). Surgical resection was performed, and histological analysis revealed nodular deposits of amyloid protein with kappa light chain predominance, without evidence of systemic involvement. This case highlights the importance of considering nodular pulmonary amyloidosis in the differential diagnosis of pulmonary nodules in patients with Sjögren's syndrome, emphasizing the need for histological evaluation to avoid misdiagnosis and inappropriate treatment.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105145"},"PeriodicalIF":1.3,"publicationDate":"2026-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12987542/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147464468","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}
Pub Date : 2026-03-13eCollection Date: 2026-03-01DOI: 10.7759/cureus.105144
Omayma El Athmani, Salah Saghir, Mustapha Azzakhmam, Anas Ayad, Rachid Abilkassem
Hepatic hemangiomas are uncommon vascular tumors in the neonatal period and are rarely reported in extremely preterm infants. Cystic variants are exceptionally rare and may exhibit atypical imaging features, making early diagnosis challenging. Spontaneous rupture with massive hemorrhage represents a life-threatening complication. We report the case of a male neonate born at 27 weeks of gestation with a birth weight of 900 g who was initially admitted to the neonatal intensive care unit for respiratory distress syndrome. During hospitalization, the infant developed recurrent severe anemia associated with progressive hepatomegaly and abdominal distension requiring multiple packed red blood cell transfusions. Clinical examination revealed marked abdominal enlargement. Abdominal radiography and contrast-enhanced computed tomography demonstrated a large multiloculated cystic hepatic mass. The clinical course rapidly deteriorated with acute hemorrhagic anemia and progressive abdominal enlargement, ultimately resulting in death. Histopathological examination of a postmortem liver biopsy confirmed a ruptured cystic hepatic hemangioma. In very preterm neonates, unexplained anemia associated with hepatomegaly should prompt consideration of rare hepatic vascular tumors. Although exceedingly rare, ruptured cystic hepatic hemangioma carries a poor prognosis in this vulnerable population.
{"title":"Fatal Hemorrhagic Rupture of a Cystic Hepatic Hemangioma in a 27-Week Preterm Neonate.","authors":"Omayma El Athmani, Salah Saghir, Mustapha Azzakhmam, Anas Ayad, Rachid Abilkassem","doi":"10.7759/cureus.105144","DOIUrl":"https://doi.org/10.7759/cureus.105144","url":null,"abstract":"<p><p>Hepatic hemangiomas are uncommon vascular tumors in the neonatal period and are rarely reported in extremely preterm infants. Cystic variants are exceptionally rare and may exhibit atypical imaging features, making early diagnosis challenging. Spontaneous rupture with massive hemorrhage represents a life-threatening complication. We report the case of a male neonate born at 27 weeks of gestation with a birth weight of 900 g who was initially admitted to the neonatal intensive care unit for respiratory distress syndrome. During hospitalization, the infant developed recurrent severe anemia associated with progressive hepatomegaly and abdominal distension requiring multiple packed red blood cell transfusions. Clinical examination revealed marked abdominal enlargement. Abdominal radiography and contrast-enhanced computed tomography demonstrated a large multiloculated cystic hepatic mass. The clinical course rapidly deteriorated with acute hemorrhagic anemia and progressive abdominal enlargement, ultimately resulting in death. Histopathological examination of a postmortem liver biopsy confirmed a ruptured cystic hepatic hemangioma. In very preterm neonates, unexplained anemia associated with hepatomegaly should prompt consideration of rare hepatic vascular tumors. Although exceedingly rare, ruptured cystic hepatic hemangioma carries a poor prognosis in this vulnerable population.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105144"},"PeriodicalIF":1.3,"publicationDate":"2026-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12989219/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147469900","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}
Pub Date : 2026-03-13eCollection Date: 2026-03-01DOI: 10.7759/cureus.105169
Yusuke Nabe, Hiroshi Mizuuchi, Masaaki Inoue, Junichi Yoshida
Primary malignant tumors of the trachea are rare, with squamous cell carcinoma (SCC) being the most frequent subtype. Due to limited data, optimal systemic therapy for unresectable or recurrent cases remains undefined. We report a case of recurrent primary tracheal SCC achieving durable complete remission with immune checkpoint inhibitor (ICI)-based combination chemotherapy. A 73-year-old man with a history of resected lung cancer was incidentally diagnosed with tracheal SCC. Following bronchoscopic tumor debulking, he underwent concurrent chemoradiotherapy. Recurrence with pulmonary metastases occurred 4 months later. He was treated with four cycles of pembrolizumab plus nab-paclitaxel and carboplatin, followed by pembrolizumab maintenance. Complete radiologic remission was achieved and sustained for over two years. This case highlights the potential of ICI-based regimens, widely used in non-small cell lung cancer, as a promising option for recurrent tracheal SCC. Multidisciplinary approaches incorporating immunotherapy may offer meaningful benefit in this rare malignancy.
{"title":"Complete Response to Chemo-Immunotherapy in Recurrent Unresectable Tracheal Squamous Cell Carcinoma: A Case Report.","authors":"Yusuke Nabe, Hiroshi Mizuuchi, Masaaki Inoue, Junichi Yoshida","doi":"10.7759/cureus.105169","DOIUrl":"https://doi.org/10.7759/cureus.105169","url":null,"abstract":"<p><p>Primary malignant tumors of the trachea are rare, with squamous cell carcinoma (SCC) being the most frequent subtype. Due to limited data, optimal systemic therapy for unresectable or recurrent cases remains undefined. We report a case of recurrent primary tracheal SCC achieving durable complete remission with immune checkpoint inhibitor (ICI)-based combination chemotherapy. A 73-year-old man with a history of resected lung cancer was incidentally diagnosed with tracheal SCC. Following bronchoscopic tumor debulking, he underwent concurrent chemoradiotherapy. Recurrence with pulmonary metastases occurred 4 months later. He was treated with four cycles of pembrolizumab plus nab-paclitaxel and carboplatin, followed by pembrolizumab maintenance. Complete radiologic remission was achieved and sustained for over two years. This case highlights the potential of ICI-based regimens, widely used in non-small cell lung cancer, as a promising option for recurrent tracheal SCC. Multidisciplinary approaches incorporating immunotherapy may offer meaningful benefit in this rare malignancy.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105169"},"PeriodicalIF":1.3,"publicationDate":"2026-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12989275/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147476821","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}
Pub Date : 2026-03-13eCollection Date: 2026-03-01DOI: 10.7759/cureus.105183
Aimad Ahmed Khamlij, Karim Hdach, Ali Habbal, Fouzia Douirek, Amra Ziadi
Acute mediastinitis is a rare but life-threatening condition, most commonly secondary to esophageal perforation. Foreign body ingestion in adults is an unusual etiology, with limited data from Morocco, where only a few cases have been reported. We report a case of mediastinitis complicating esophageal perforation following accidental foreign body ingestion in a Moroccan patient, highlighting diagnostic challenges and management in a resource-limited setting. We report the case of a 38-year-old patient admitted with septic shock, complicated by dysphagia and epigastric pain, five days after accidental foreign body ingestion. A cervicothoracic CT scan revealed esophageal perforation complicated by mediastinitis and inhalation pneumonia. Emergency surgical management consisted of a Kocher cervicotomy with mediastinal drainage, combined with early broad-spectrum antibiotic therapy, which led to a favorable postoperative outcome. This case from Morocco underscores the importance of early clinical suspicion, prompt CT imaging, and aggressive medico-surgical management in improving outcomes, even in delayed presentations. It contributes to the growing body of regional literature on foreign body-induced mediastinitis in North Africa.
{"title":"From Ingestion to Septic Shock: A Case Report on Esophageal Perforation and Mediastinitis Following Foreign Body Ingestion.","authors":"Aimad Ahmed Khamlij, Karim Hdach, Ali Habbal, Fouzia Douirek, Amra Ziadi","doi":"10.7759/cureus.105183","DOIUrl":"10.7759/cureus.105183","url":null,"abstract":"<p><p>Acute mediastinitis is a rare but life-threatening condition, most commonly secondary to esophageal perforation. Foreign body ingestion in adults is an unusual etiology, with limited data from Morocco, where only a few cases have been reported. We report a case of mediastinitis complicating esophageal perforation following accidental foreign body ingestion in a Moroccan patient, highlighting diagnostic challenges and management in a resource-limited setting. We report the case of a 38-year-old patient admitted with septic shock, complicated by dysphagia and epigastric pain, five days after accidental foreign body ingestion. A cervicothoracic CT scan revealed esophageal perforation complicated by mediastinitis and inhalation pneumonia. Emergency surgical management consisted of a Kocher cervicotomy with mediastinal drainage, combined with early broad-spectrum antibiotic therapy, which led to a favorable postoperative outcome. This case from Morocco underscores the importance of early clinical suspicion, prompt CT imaging, and aggressive medico-surgical management in improving outcomes, even in delayed presentations. It contributes to the growing body of regional literature on foreign body-induced mediastinitis in North Africa.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105183"},"PeriodicalIF":1.3,"publicationDate":"2026-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12987540/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147464441","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}
Pub Date : 2026-03-12eCollection Date: 2026-03-01DOI: 10.7759/cureus.105124
Mohammed Alenezi, Salamah Ayyad, Thunayan Alemairi
Osteonecrosis of the femoral head is a well-recognized musculoskeletal complication of sickle cell disease (SCD) that frequently results in early joint destruction and functional disability in young patients. The coexistence of avascular necrosis and septic arthritis in SCD patients is uncommon and presents significant diagnostic and therapeutic challenges. We report the case of a 24-year-old male patient with sickle cell disease who developed septic arthritis of the hip following femoral head core decompression, ultimately requiring staged total hip arthroplasty.
{"title":"Staged Total Hip Arthroplasty for Septic Hip Following Core Decompression in Sickle Cell-Related Osteonecrosis: A Case Report and Review of the Literature.","authors":"Mohammed Alenezi, Salamah Ayyad, Thunayan Alemairi","doi":"10.7759/cureus.105124","DOIUrl":"10.7759/cureus.105124","url":null,"abstract":"<p><p>Osteonecrosis of the femoral head is a well-recognized musculoskeletal complication of sickle cell disease (SCD) that frequently results in early joint destruction and functional disability in young patients. The coexistence of avascular necrosis and septic arthritis in SCD patients is uncommon and presents significant diagnostic and therapeutic challenges. We report the case of a 24-year-old male patient with sickle cell disease who developed septic arthritis of the hip following femoral head core decompression, ultimately requiring staged total hip arthroplasty.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105124"},"PeriodicalIF":1.3,"publicationDate":"2026-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12981732/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147464432","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}
Pub Date : 2026-03-12eCollection Date: 2026-03-01DOI: 10.7759/cureus.105097
Pasala Jayavardhan Yadav, Gils Thampi, Nagakumar J S
Introduction Sacroiliitis is a well-recognized cause of axial low back pain and significantly contributes to chronic cases seen in orthopedic and pain clinics. While intra-articular corticosteroid injections provide established short-term symptom relief, their long-term effectiveness remains variable. Platelet-rich plasma (PRP) has emerged as a biological alternative with regenerative potential, and viscosupplementation using hyaluronic acid offers viscoelastic and anti-inflammatory effects that may enhance joint function. This study aimed to compare the therapeutic efficacy of intra-articular corticosteroid, PRP, and viscosupplement injections in treating sacroiliitis. Materials and methods This retrospective comparative study included 60 adults with clinically and magnetic resonance imaging (MRI)-confirmed sacroiliitis who were treated between January 2022 and December 2024. Patients received one of the following treatments: fluoroscopy-guided intra-articular injection of 40 mg methylprednisolone acetate combined with lidocaine (steroid group; n=20), 5 mL of autologous PRP prepared using a standardized double-spin centrifugation protocol (PRP group; n=20), or intra-articular hyaluronic acid viscosupplementation (viscosupplement group; n=20). Pain and functional status were assessed using the Visual Analog Scale (VAS) and Oswestry Disability Index (ODI) at baseline, one week, one month, three months, and six months. Statistical analysis was conducted using repeated measures and one-way analysis of variance (ANOVA). Results Baseline VAS scores were comparable among the steroid (7.9±0.8), PRP (7.8±0.9), and viscosupplement (7.8±0.7) groups (p>0.05). The steroid group demonstrated greater early pain reduction at one week (4.6±0.9) compared to the PRP (6.2±0.8) and viscosupplement (5.8±0.9) groups. At six months, the PRP group showed the greatest improvement, with a mean VAS of 3.8±1.0, followed by the viscosupplement group (4.3±1.1), while the steroid group had higher scores (5.1±1.2) (p<0.05). Similarly, the mean ODI at six months was lowest in the PRP group (31.9±6.8%), followed by the viscosupplement (35.6±7.2%) and steroid groups (40.3±7.5%) (p<0.05). All groups showed significant improvement from baseline (p<0.001). No major complications were observed. Conclusion Intra-articular injections of corticosteroids, PRP, and viscosupplements effectively reduce pain and disability in sacroiliitis. Corticosteroids provide rapid early symptom relief, while PRP demonstrates superior mid-term improvement. Viscosupplementation offers sustained clinical benefits and represents a safe and effective therapeutic alternative.
骶髂炎是一种公认的引起轴性腰痛的原因,在骨科和疼痛诊所中,它是慢性病例的重要原因。虽然关节内皮质类固醇注射提供了确定的短期症状缓解,但其长期有效性仍不确定。富血小板血浆(PRP)已成为具有再生潜力的生物替代品,使用透明质酸补充粘胶具有粘弹性和抗炎作用,可以增强关节功能。本研究旨在比较关节内皮质类固醇、PRP和粘剂补充注射治疗骶髂炎的疗效。材料和方法本回顾性比较研究包括60名临床和磁共振成像(MRI)确诊的成人骶髂炎患者,他们在2022年1月至2024年12月期间接受了治疗。患者接受以下治疗之一:在透视引导下关节内注射醋酸甲基强的松龙联合利多卡因40 mg(类固醇组,n=20),采用标准化双旋离心方案制备的自体PRP 5 mL (PRP组,n=20),或关节内补充透明质酸粘胶(粘胶补充组,n=20)。在基线、1周、1个月、3个月和6个月时,采用视觉模拟量表(VAS)和Oswestry残疾指数(ODI)评估疼痛和功能状态。采用重复测量法和单因素方差分析(ANOVA)进行统计分析。结果类固醇组(7.9±0.8)、PRP组(7.8±0.9)和粘剂组(7.8±0.7)的基线VAS评分具有可比性(p < 0.05)。与PRP组(6.2±0.8)和粘剂补充组(5.8±0.9)相比,类固醇组在一周内表现出更大的早期疼痛减轻(4.6±0.9)。在6个月时,PRP组表现出最大的改善,平均VAS为3.8±1.0,其次是粘补充剂组(4.3±1.1),而类固醇组得分更高(5.1±1.2)(p
{"title":"Therapeutic Evaluation of Intra-articular Platelet-Rich Plasma, Steroid, and Viscosupplement Injections for Sacroiliitis: A Retrospective Comparative Study.","authors":"Pasala Jayavardhan Yadav, Gils Thampi, Nagakumar J S","doi":"10.7759/cureus.105097","DOIUrl":"10.7759/cureus.105097","url":null,"abstract":"<p><p>Introduction Sacroiliitis is a well-recognized cause of axial low back pain and significantly contributes to chronic cases seen in orthopedic and pain clinics. While intra-articular corticosteroid injections provide established short-term symptom relief, their long-term effectiveness remains variable. Platelet-rich plasma (PRP) has emerged as a biological alternative with regenerative potential, and viscosupplementation using hyaluronic acid offers viscoelastic and anti-inflammatory effects that may enhance joint function. This study aimed to compare the therapeutic efficacy of intra-articular corticosteroid, PRP, and viscosupplement injections in treating sacroiliitis. Materials and methods This retrospective comparative study included 60 adults with clinically and magnetic resonance imaging (MRI)-confirmed sacroiliitis who were treated between January 2022 and December 2024. Patients received one of the following treatments: fluoroscopy-guided intra-articular injection of 40 mg methylprednisolone acetate combined with lidocaine (steroid group; n=20), 5 mL of autologous PRP prepared using a standardized double-spin centrifugation protocol (PRP group; n=20), or intra-articular hyaluronic acid viscosupplementation (viscosupplement group; n=20). Pain and functional status were assessed using the Visual Analog Scale (VAS) and Oswestry Disability Index (ODI) at baseline, one week, one month, three months, and six months. Statistical analysis was conducted using repeated measures and one-way analysis of variance (ANOVA). Results Baseline VAS scores were comparable among the steroid (7.9±0.8), PRP (7.8±0.9), and viscosupplement (7.8±0.7) groups (p>0.05). The steroid group demonstrated greater early pain reduction at one week (4.6±0.9) compared to the PRP (6.2±0.8) and viscosupplement (5.8±0.9) groups. At six months, the PRP group showed the greatest improvement, with a mean VAS of 3.8±1.0, followed by the viscosupplement group (4.3±1.1), while the steroid group had higher scores (5.1±1.2) (p<0.05). Similarly, the mean ODI at six months was lowest in the PRP group (31.9±6.8%), followed by the viscosupplement (35.6±7.2%) and steroid groups (40.3±7.5%) (p<0.05). All groups showed significant improvement from baseline (p<0.001). No major complications were observed. Conclusion Intra-articular injections of corticosteroids, PRP, and viscosupplements effectively reduce pain and disability in sacroiliitis. Corticosteroids provide rapid early symptom relief, while PRP demonstrates superior mid-term improvement. Viscosupplementation offers sustained clinical benefits and represents a safe and effective therapeutic alternative.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105097"},"PeriodicalIF":1.3,"publicationDate":"2026-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12981201/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147464479","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}