Back to Search Start Over

A Rare Case with Recurrent Abdominal Pain as the First Symptom: AL Amyloidosis with Colon Involvement Combined with Pulmonary Adenocarcinoma

Authors :
Wei J
Hu Y
Lu C
Hu M
Wang Q
Source :
Journal of Inflammation Research, Vol Volume 18, Pp 53-59 (2025)
Publication Year :
2025
Publisher :
Dove Medical Press, 2025.

Abstract

Jiaojiao Wei, Yibing Hu, Chong Lu, Minli Hu, Qunying Wang Department of Gastroenterology, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, Zhejiang, People’s Republic of ChinaCorrespondence: Qunying Wang, Department of Gastroenterology, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, Zhejiang, People’s Republic of China, Email wqy616717@126.comBackground: Amyloidosis combined with lung cancer is a rare occurrence. To date, there are no reported cases of amyloid light-chain(AL) amyloidosis solely affecting the colon combined with pulmonary adenocarcinoma.Case Summary: Here, we describe a case of a 66-year-old woman who presented with recurrent abdominal pain and was eventually diagnosed with AL amyloidosis with colon involvement and pulmonary adenocarcinoma. We also review the relevant literature and discuss the relationship between amyloidosis and lung malignancies. Significantly, lung cancer may contribute to the deposition of amyloid through paraneoplastic mechanisms. And in published case reports, the pathological type of lung cancer associated with AL amyloidosis was all adenocarcinoma.Conclusion: Such cases are rare but provide new insights into the relationship between amyloidosis and lung malignancies. The mechanism of amyloid protein deposition in relation to lung cancer or malignancies remains unknown, further research in this field is warranted.Keywords: amyloidosis, adenocarcinoma, lung cancer, comorbidity

Details

Language :
English
ISSN :
11787031
Volume :
ume 18
Database :
Directory of Open Access Journals
Journal :
Journal of Inflammation Research
Publication Type :
Academic Journal
Accession number :
edsdoj.f8f9666d8164fedaed36bf3ad2394a9
Document Type :
article