Table 1_Idiopathic AA amyloidosis presenting with initial abdominal pain: a case report and literature review.docx
<p>Amyloidosis is a rare disease, often secondary to chronic inflammation or autoimmune disorders, with an unclear etiology in some cases. Herein, we report a 67-year-old male patient presenting with recurrent abdominal pain and multi-system involvement. The diagnosis of AA amyloidosis was con...
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2025
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| _version_ | 1851483696115220480 |
|---|---|
| author | Pianpian Xia (22070450) |
| author2 | Deliang Liu (2165083) Feihong Deng (4988315) Dalian Ou (22070453) Mingyang Deng (504326) |
| author2_role | author author author author |
| author_facet | Pianpian Xia (22070450) Deliang Liu (2165083) Feihong Deng (4988315) Dalian Ou (22070453) Mingyang Deng (504326) |
| author_role | author |
| dc.creator.none.fl_str_mv | Pianpian Xia (22070450) Deliang Liu (2165083) Feihong Deng (4988315) Dalian Ou (22070453) Mingyang Deng (504326) |
| dc.date.none.fl_str_mv | 2025-08-18T05:16:32Z |
| dc.identifier.none.fl_str_mv | 10.3389/fmed.2025.1640436.s001 |
| dc.relation.none.fl_str_mv | https://figshare.com/articles/dataset/Table_1_Idiopathic_AA_amyloidosis_presenting_with_initial_abdominal_pain_a_case_report_and_literature_review_docx/29928857 |
| dc.rights.none.fl_str_mv | CC BY 4.0 info:eu-repo/semantics/openAccess |
| dc.subject.none.fl_str_mv | Foetal Development and Medicine abdominal pain AA amyloidosis diagnosis etiology serum amyloid A protein gastrointestinal diseases |
| dc.title.none.fl_str_mv | Table 1_Idiopathic AA amyloidosis presenting with initial abdominal pain: a case report and literature review.docx |
| dc.type.none.fl_str_mv | Dataset info:eu-repo/semantics/publishedVersion dataset |
| description | <p>Amyloidosis is a rare disease, often secondary to chronic inflammation or autoimmune disorders, with an unclear etiology in some cases. Herein, we report a 67-year-old male patient presenting with recurrent abdominal pain and multi-system involvement. The diagnosis of AA amyloidosis was confirmed by Congo red staining of small intestinal mucosal and bone marrow biopsies. Despite comprehensive screening, no definite etiology was identified. This case highlights that amyloidosis should be considered in patients with unexplained abdominal pain and multisystem abnormalities, and early tissue biopsy is crucial for diagnosis.</p> |
| eu_rights_str_mv | openAccess |
| id | Manara_12c9dc18b373ab927b9da99d4b933e1b |
| identifier_str_mv | 10.3389/fmed.2025.1640436.s001 |
| network_acronym_str | Manara |
| network_name_str | ManaraRepo |
| oai_identifier_str | oai:figshare.com:article/29928857 |
| publishDate | 2025 |
| repository.mail.fl_str_mv | |
| repository.name.fl_str_mv | |
| repository_id_str | |
| rights_invalid_str_mv | CC BY 4.0 |
| spelling | Table 1_Idiopathic AA amyloidosis presenting with initial abdominal pain: a case report and literature review.docxPianpian Xia (22070450)Deliang Liu (2165083)Feihong Deng (4988315)Dalian Ou (22070453)Mingyang Deng (504326)Foetal Development and Medicineabdominal painAA amyloidosisdiagnosisetiologyserum amyloid A proteingastrointestinal diseases<p>Amyloidosis is a rare disease, often secondary to chronic inflammation or autoimmune disorders, with an unclear etiology in some cases. Herein, we report a 67-year-old male patient presenting with recurrent abdominal pain and multi-system involvement. The diagnosis of AA amyloidosis was confirmed by Congo red staining of small intestinal mucosal and bone marrow biopsies. Despite comprehensive screening, no definite etiology was identified. This case highlights that amyloidosis should be considered in patients with unexplained abdominal pain and multisystem abnormalities, and early tissue biopsy is crucial for diagnosis.</p>2025-08-18T05:16:32ZDatasetinfo:eu-repo/semantics/publishedVersiondataset10.3389/fmed.2025.1640436.s001https://figshare.com/articles/dataset/Table_1_Idiopathic_AA_amyloidosis_presenting_with_initial_abdominal_pain_a_case_report_and_literature_review_docx/29928857CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/299288572025-08-18T05:16:32Z |
| spellingShingle | Table 1_Idiopathic AA amyloidosis presenting with initial abdominal pain: a case report and literature review.docx Pianpian Xia (22070450) Foetal Development and Medicine abdominal pain AA amyloidosis diagnosis etiology serum amyloid A protein gastrointestinal diseases |
| status_str | publishedVersion |
| title | Table 1_Idiopathic AA amyloidosis presenting with initial abdominal pain: a case report and literature review.docx |
| title_full | Table 1_Idiopathic AA amyloidosis presenting with initial abdominal pain: a case report and literature review.docx |
| title_fullStr | Table 1_Idiopathic AA amyloidosis presenting with initial abdominal pain: a case report and literature review.docx |
| title_full_unstemmed | Table 1_Idiopathic AA amyloidosis presenting with initial abdominal pain: a case report and literature review.docx |
| title_short | Table 1_Idiopathic AA amyloidosis presenting with initial abdominal pain: a case report and literature review.docx |
| title_sort | Table 1_Idiopathic AA amyloidosis presenting with initial abdominal pain: a case report and literature review.docx |
| topic | Foetal Development and Medicine abdominal pain AA amyloidosis diagnosis etiology serum amyloid A protein gastrointestinal diseases |