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AME Case Reports|October 14, 2026
18F-AlF-NOTA-FAPI-04 PET/CT as a complementary tool for detecting occult signet-ring cell gastric adenocarcinoma when FDG imaging is inconclusive: a case reportCheng Yuan, Mingzhe Lai, Yanzhi Fu, et al.AME Case Reports|October 14, 2026
Classical Hodgkin lymphoma as a second malignancy in a patient with cervical squamous cell carcinoma following chemoradiotherapy: a case reportZhemei Xin, Chengshi WangAME Case Reports|October 14, 2026
Staged total arch repair for acute aortic dissection using physician-modified fenestrated thoracic endovascular aortic repair: a case reportAtsutaka Aratame, Daisuke Kaku, Toshio BabaAME Case Reports|October 14, 2026
Prolonged survival in a 57-year-old female with RB1-wildtype transformed small-cell lung cancer treated with immunochemotherapy and antiangiogenic combined therapy: a case reportLiping Kang, Liping Zhao, Xiaolong Chen, et al.AME Case Reports|October 14, 2026
Urogenital abscess with a complex etiology: a case reportNatalie Grace Narcelles, Afolabi David Akinpelu, Michael Duke SarapAME Case Reports|October 14, 2026
Presumed ocular tuberculosis presenting as a subfoveal choroidal granuloma in a healthcare professional: a case reportHuda Abdul Halim, Shelina Oli Mohamed, Nur Amirah ShibraumalisiAME Case Reports|October 14, 2026
Where did the iron go?-a case report of a patient with severe iron deficiency anemia despite parenteral and oral iron supplementation due to semaglutide applicationStjepan Šimić, Jure Ćurić, Filip Sedlić, et al.AME Case Reports|October 14, 2026
Conservative management of a retained bullet in the right atrioventricular groove following a penetrating thoracic gunshot wound: a case reportSira Laohathai, Jakraphan Yu, Thanga SaravananAME Case Reports|October 14, 2026
Hypo-osmotic swelling test guided sperm selection followed by intracytoplasmic sperm injection in two men with multiple morphological abnormalities of the sperm flagella associated with SPEF2 and CFAP251 variants: two case reportsHaiqing Deng, Tingting ZhengAME Case Reports|October 14, 2026
Neonatal autosomal recessive dystrophic epidermolysis bullosa caused by compound heterozygous COL7A1 variants: a case reportZhongfen Cao, Cheng Peng, Xueyan Du, et al.Pageof 74