Medical ReportsPub Date : 2025-07-09DOI: 10.1016/j.hmedic.2025.100311
Ahmad Jradi , Mohamad Al Qassab , Sereina Ghattas , Nadim Chaarani , Philippe Attieh , Karam Karam , Walid Salamoun
{"title":"Confronting a colossal challenge: A case report and literature review on the diagnosis and management of a 40 cm, 3.3 kg phyllodes tumor","authors":"Ahmad Jradi , Mohamad Al Qassab , Sereina Ghattas , Nadim Chaarani , Philippe Attieh , Karam Karam , Walid Salamoun","doi":"10.1016/j.hmedic.2025.100311","DOIUrl":"10.1016/j.hmedic.2025.100311","url":null,"abstract":"<div><div>With a peak incidence in women of 45–49 years old, phyllodes tumors (PT) are uncommon fibroepithelial neoplasms that make up less than 1 % of all breast tumors. Based on histological features, these tumors are categorized into benign, borderline, and malignant subtypes, with the malignant subtype having the worst prognosis and highest chance of recurrence. Diagnosing PT remains challenging due to its similarities with fibroadenomas (FA), necessitating the use of core needle biopsy for accurate differentiation. Our 59-year-old female patient described in this report had a borderline PTs that had grown to a remarkable 40 × 35 × 10 cm size and was causing serious clinical issues, such as skin ulceration. Following a modified mastectomy, an intermediate-grade PT with negative surgical margins was verified by histological examination. Since the tumor was within 1 mm from the posterior margin, adjuvant radiation therapy was recommended. A comprehensive review of the literature was performed to explore the diagnostic challenges, imaging modalities, histopathological features, and treatment approaches for PT, including surgical resection, the role of radiation therapy, and the limited efficacy of chemotherapy. To guarantee the best possible results for patients with PTs, this case emphasizes the need of early detection and the necessity for precise surgical intervention.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"13 ","pages":"Article 100311"},"PeriodicalIF":0.0,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144597141","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Medical ReportsPub Date : 2025-07-09DOI: 10.1016/j.hmedic.2025.100313
Chakib Khoury , Rebal Nahas , Karam Karam , Emanuel-Youssef Dib , Elias Fiani
{"title":"A polypoid mucosa-associated lymphoid tissue lymphoma causing gastric outlet obstruction: A case report and literature review","authors":"Chakib Khoury , Rebal Nahas , Karam Karam , Emanuel-Youssef Dib , Elias Fiani","doi":"10.1016/j.hmedic.2025.100313","DOIUrl":"10.1016/j.hmedic.2025.100313","url":null,"abstract":"<div><div>Gastric mucosa-associated lymphoid tissue (MALT) lymphoma is the most frequent extra-nodal lymphoma type of the gastrointestinal tract. MALT lymphomas typically present with non-specific symptoms of nausea and epigastric discomfort. Lesions are commonly situated within the antrum or along the greater and lesser curvatures. Known to be highly associated with Helicobacter pylori infection, eradication therapy has been the standard in treating gastric MALT lymphomas. We herein present a case of a 34-year-old male with symptoms of gastric outlet obstruction (GOO), found to have a peri-pyloric lesion obstructing the stomach, treated with immediate endoscopic mucosal resection (EMR) via hot-snare polypectomy and H. pylori eradication therapy. Follow-up endoscopies at 3 and 12 months showed no recurrence. That said, gastric polypectomy is the gold standard of management of gastric MALT lymphoma that present with obstructive symptoms.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"13 ","pages":"Article 100313"},"PeriodicalIF":0.0,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144597143","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Medical ReportsPub Date : 2025-07-08DOI: 10.1016/j.hmedic.2025.100312
Salma Barakat , Sarah Ahmed , Ahmed Rafei , Rawan A. Bedab , Abdelmounem E. Abdo
{"title":"Spontaneous passage of a retained endoscopic capsule prior to scheduled surgery in a Crohn’s disease patient: A case report","authors":"Salma Barakat , Sarah Ahmed , Ahmed Rafei , Rawan A. Bedab , Abdelmounem E. Abdo","doi":"10.1016/j.hmedic.2025.100312","DOIUrl":"10.1016/j.hmedic.2025.100312","url":null,"abstract":"<div><h3>Background</h3><div>Video capsule endoscopy (VCE) is a noninvasive tool used to evaluate small bowel diseases, including Crohn’s disease, suspected small bowel bleeding, malabsorption, and chronic diarrhea. A known complication is capsule retention (CR), particularly in patients with established Crohn’s disease and undetected strictures. While CR often requires endoscopic or surgical removal, spontaneous passage has been reported following medical therapy.</div></div><div><h3>Case summary</h3><div>We present the first documented case in Sudan of a 28-year-old male with Crohn’s disease who experienced capsule retention, followed by spontaneous passage. The patient had a 7-year history of chronic diarrhea, weight loss, and post-defecation abdominal pain. Initial imaging and endoscopy were inconclusive. A small bowel follow-through confirmed luminal patency, and VCE was performed, revealing classic Crohn’s features and suggesting a terminal ileal stricture. Two weeks later, X-ray showed the capsule retained in the right colon, and surgery was planned. However, a follow-up radiograph before surgery confirmed spontaneous passage, likely aided by corticosteroid and mesalamine therapy.</div></div><div><h3>Conclusion</h3><div>This case underscores the importance of evaluating for strictures before VCE in Crohn’s patients. Conservative treatment may promote capsule passage in selected cases, avoiding invasive intervention. Use of patency capsules and cross-sectional imaging is recommended to minimize retention risk.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"13 ","pages":"Article 100312"},"PeriodicalIF":0.0,"publicationDate":"2025-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144614274","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Medical ReportsPub Date : 2025-07-07DOI: 10.1016/j.hmedic.2025.100310
O. Lahjouji , I. Chaouche , H. Ouazzani , A. Akammar , N. El Bouardi , M. Haloua , M.Y. Alaoui Lamrani , M. Boubbou , M. Maâroufi , B. Alami
{"title":"Neurosarcoidosis masquerading as cerebral metastasis lesion: Case report","authors":"O. Lahjouji , I. Chaouche , H. Ouazzani , A. Akammar , N. El Bouardi , M. Haloua , M.Y. Alaoui Lamrani , M. Boubbou , M. Maâroufi , B. Alami","doi":"10.1016/j.hmedic.2025.100310","DOIUrl":"10.1016/j.hmedic.2025.100310","url":null,"abstract":"<div><div>Sarcoidosis is a chronic multisystemic granulomatous disease that is still of an unknown etiology. Neurosarcoidosis refers to the manifestations of sarcoidosis affecting central or peripheral nervous system. Due to its multiorgan tropism, sarcoidosis can mimic a metastatic disease. We report a case of a patient who was initially suspected of having a cerebral metastatic lesion. Subsequent investigations suggested an association with multiple lung lesions, but no primary cancer was identified. Histopathological examination of a biopsied lung nodule revealed noncaseating granulomas, establishing an unexpected diagnosis of sarcoidosis. Following this diagnosis, steroid treatment was initiated, resulting in a favorable response.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"13 ","pages":"Article 100310"},"PeriodicalIF":0.0,"publicationDate":"2025-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144571766","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Medical ReportsPub Date : 2025-07-05DOI: 10.1016/j.hmedic.2025.100303
Tomas Leng , Ayesha Ali
{"title":"Spinal epidural abscess in infants: Case report and review of the literature","authors":"Tomas Leng , Ayesha Ali","doi":"10.1016/j.hmedic.2025.100303","DOIUrl":"10.1016/j.hmedic.2025.100303","url":null,"abstract":"<div><div>Spinal epidural abscess (SEA) is an uncommon but serious condition in children, where timely diagnosis is essential to avoid permanent neurological complications. Diagnosing SEA in pediatric patients, particularly in infants, is challenging due to nonspecific symptoms such as fever and pain, which are often difficult to interpret and can lead to delayed or missed diagnoses. This report details the case of a 10-month-old otherwise healthy infant with an extensive SEA, where fluorine-18 fluorodeoxyglucose PET/CT (F-FDG PET CT) was effectively used to confirm the diagnosis. Additionally, we conducted a comprehensive literature review from January 2000 to October 2024 to explore clinical presentations and imaging considerations unique to infants with SEA. Of the 124 cases reviewed, 13 met our inclusion criteria. The most common symptoms were fever and irritability, followed by motor deficits. The primary pathogen was MSSA, affecting the cervical spine in most cases, and the majority of infants received antibiotics, with most undergoing neurosurgical intervention, and no deaths were reported in the cohort. This case, along with the review, underscores the importance of early recognition and advanced imaging approaches in enhancing diagnostic accuracy and improving outcomes for pediatric SEA. F-FDG PET CT can be diagnostically useful in certain infant cases of occult bacteremia where no obvious infection source is identified.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"13 ","pages":"Article 100303"},"PeriodicalIF":0.0,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144571194","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Medical ReportsPub Date : 2025-07-05DOI: 10.1016/j.hmedic.2025.100309
Ahmed Basuoni , Marwa Ahmed , Karim Abdel Hakim , Sulaiman Al Maqbali , Waleed DawElbeit
{"title":"Pericardial decompression syndrome after small-volume pericardiocentesis: A case report when even less is too much","authors":"Ahmed Basuoni , Marwa Ahmed , Karim Abdel Hakim , Sulaiman Al Maqbali , Waleed DawElbeit","doi":"10.1016/j.hmedic.2025.100309","DOIUrl":"10.1016/j.hmedic.2025.100309","url":null,"abstract":"<div><h3>Background</h3><div>Pericardial decompression syndrome (PDS) is a rare but potentially life-threatening complication following pericardial drainage, typically associated with large-volume effusion removal of more than 1 L within 1 h.</div></div><div><h3>Case summary</h3><div>We report the case of a 62-year-old man with metastatic thymic carcinoma and severe mitral regurgitation who developed acute pulmonary edema and transient left ventricular dysfunction following pericardiocentesis. Despite draining only 600 mL of pericardial fluid, the patient developed respiratory failure, pulmonary edema and required mechanical ventilation. Echocardiography revealed a drop in ejection fraction and elevated filling pressures. Prompt recognition and supportive management, including diuresis and intensive care monitoring, led to full recovery of cardiac function within days.</div></div><div><h3>Conclusion</h3><div>This case highlights that PDS may develop even after small-volume pericardial drainage in patients with compromised cardiac reserve. Proposed mechanisms include preload-afterload mismatch, myocardial stunning, and adrenergic withdrawal. Awareness, early diagnosis, and careful pericardial fluid removal are key to preventing and managing PDS even in draining small amount especially with underlying structural heart disease or baseline reduced left ventricular function.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"13 ","pages":"Article 100309"},"PeriodicalIF":0.0,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144571192","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Medical ReportsPub Date : 2025-07-05DOI: 10.1016/j.hmedic.2025.100308
Bipneet Singh , Jack Visser , Sakshi Bai , Jahnavi Ethakota , Palak Grover , Gurleen Kaur , Syed-Mohammed Jafri
{"title":"Intestinal spirochetosis","authors":"Bipneet Singh , Jack Visser , Sakshi Bai , Jahnavi Ethakota , Palak Grover , Gurleen Kaur , Syed-Mohammed Jafri","doi":"10.1016/j.hmedic.2025.100308","DOIUrl":"10.1016/j.hmedic.2025.100308","url":null,"abstract":"<div><div>Intestinal spirochetosis involves the colonization of the colonic epithelium by Brachyspira. Patients may be asymptomatic or present with diarrhea, abdominal pain, and bloating. It generally affects immunocompromised individuals. Diagnosis requires colonoscopy with biopsies and specific staining, often missed due to its rarity. Treatment typically involves metronidazole, with macrolides as alternatives, but relapse can occur, necessitating better follow-up and documentation. We present four cases that highlight diverse presentations and responses to treatment. A 36-year-old male with multiple sclerosis (MS) and psoriasis, who experienced symptom resolution with metronidazole; a 23-year-old male with abdominal pain and diarrhea, who improved with clarithromycin; an 86-year-old diabetic with chronic diarrhea who responded to metronidazole but experienced a relapse; and a 54-year-old male with HIV-AIDS, who was treated for concurrent H. pylori with no recurrence. Diagnostic challenges arise due to symptom variability and slow growth on culture. Treatment with metronidazole is effective but prone to relapse, possibly due to spirochete translocation within colonic crypts. More research is needed to establish clear diagnostic markers, understand epidemiological patterns, and develop effective long-term treatments.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"13 ","pages":"Article 100308"},"PeriodicalIF":0.0,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144597142","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Medical ReportsPub Date : 2025-07-05DOI: 10.1016/j.hmedic.2025.100306
Nikita Kashyap , Debarati Ray , Divya Nadiminti , S. Aravindan , Jay Gopal Ray
{"title":"Ewing sarcoma of maxilla masquerading as odontogenic lesion; And role of NKX2.2 for confirmatory diagnosis: A rare case report","authors":"Nikita Kashyap , Debarati Ray , Divya Nadiminti , S. Aravindan , Jay Gopal Ray","doi":"10.1016/j.hmedic.2025.100306","DOIUrl":"10.1016/j.hmedic.2025.100306","url":null,"abstract":"<div><div>Ewing sarcoma (ES), defined as a malignant small round blue cell neoplasm of bone and soft tissue occurs most frequently in children and young adults. ES is an aggressive tumor showing rapid growth and metastasis. It has been documented to strike the skull, supraclavicular region, parotid region, orbital floor, nasal cavity, maxilla, mandible, and zygoma in the head and neck region. The incidence of ES as a primary lesion in the head and neck region is reportedly 2–3 % of all cases only. The differential diagnoses for these tumors include alveolar rhabdomyosarcoma, desmoplastic small round cell tumor, poorly differentiated round cell synovial sarcoma, small cell osteosarcoma, and mesenchymal chondrosarcoma. Here we report a case of primary Ewing sarcoma involving the maxilla in a 12 year male with its clinical, radiological, histopathological findings, initially misdiagnosed as a benign entity. Special emphasis on hallmark immunohistochemical features are also discussed.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"13 ","pages":"Article 100306"},"PeriodicalIF":0.0,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144588929","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Medical ReportsPub Date : 2025-07-04DOI: 10.1016/j.hmedic.2025.100304
Toni Habib , Chloe Lahoud , Zaid Khamis , Muhammad Abdullah , Hadi Itani , Hassan Al Moussawi
{"title":"Disseminated intravascular coagulation: An unexpected signpost to ulcerative colitis: A case report","authors":"Toni Habib , Chloe Lahoud , Zaid Khamis , Muhammad Abdullah , Hadi Itani , Hassan Al Moussawi","doi":"10.1016/j.hmedic.2025.100304","DOIUrl":"10.1016/j.hmedic.2025.100304","url":null,"abstract":"<div><div>Ulcerative colitis (UC) is a chronic inflammatory bowel disease with varied clinical presentations. We report a case of a 25-year-old male who presented with abdominal pain and bloody diarrhea, initially treated as infectious colitis. The patient's condition rapidly deteriorated, developing pancytopenia and coagulation abnormalities consistent with DIC. Subsequent colonoscopy and biopsies confirmed severe UC. This case is unique as DIC was an early manifestation of an undiagnosed UC. It highlights the importance of considering inflammatory bowel disease in the differential diagnosis of acute bloody diarrhea, even in patients without prior gastrointestinal history. It also underscores the rare occurrence of DIC as an early feature of UC, emphasizing the need for vigilant monitoring of coagulation parameters in severe colitis cases.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"13 ","pages":"Article 100304"},"PeriodicalIF":0.0,"publicationDate":"2025-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144556918","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Medical ReportsPub Date : 2025-07-03DOI: 10.1016/j.hmedic.2025.100305
Dmytro Ishchenko
{"title":"Progressive neck deformation after intramedular cervical tumor removal by laminoplasty approach","authors":"Dmytro Ishchenko","doi":"10.1016/j.hmedic.2025.100305","DOIUrl":"10.1016/j.hmedic.2025.100305","url":null,"abstract":"<div><div>Posterior approaches are usually used for the removal of tumors localized in the spinal canal, employing laminectomy techniques with the possibility of subsequent laminoplasty. However, even when bone defects are replaced with autografts, studies have shown a high likelihood of postoperative deformities, particularly in cases involving multisegment laminoplasty and radiotherapy. This risk increases with multisegmented laminoplasty and subsequent radiotherapy exposure. This study presents a clinical case of treating a patient with an intramedullary tumor from C2-Th1 after surgery using the laminoplasty technique, followed by adjuvant radiotherapy. After treatment, the patient developed pathological kyphosis of the cervical spine, with a Cobb angle of 82°. A comprehensive treatment approach was employed, which included fixation and traction in a HALO-vest apparatus, followed by anterior corporodesis and posterior occipitospinal fusion to achieve satisfactory correction and prevent further deformities and secondary spinal cord injuries. Deformities are a common complication of laminoplasty without additional stabilization. The contributing factors include the use of multilevel approaches, adjuvant radiotherapy, and pre-existing segmental instability. Careful planning is required to prevent pathological kyphosis and secondary spinal cord injury. This planning should consider the volume of bone defects, fixation techniques, subsequent treatment, initial range of motion, and type of primary physiological curvature.</div></div>","PeriodicalId":100908,"journal":{"name":"Medical Reports","volume":"13 ","pages":"Article 100305"},"PeriodicalIF":0.0,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144556919","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}