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Localized Insulin-Derived Amyloidosis in Diabetes Mellitus Type 1 Patient: A Case Report
Localized insulin-derived amyloidosis (LIDA) is a rare local complication of subcutaneous insulin application occurring in patients with diabetes type 1 and 2. A 45-year-old woman with an 11-year history of insulin-dependent diabetes mellitus type 1 underwent a mini-abdominoplasty and excision of a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378134/ https://www.ncbi.nlm.nih.gov/pubmed/37510159 http://dx.doi.org/10.3390/diagnostics13142415 |
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author | Hrudka, Jan Sticová, Eva Krbcová, Magdaléna Schwarzmannová, Klára |
author_facet | Hrudka, Jan Sticová, Eva Krbcová, Magdaléna Schwarzmannová, Klára |
author_sort | Hrudka, Jan |
collection | PubMed |
description | Localized insulin-derived amyloidosis (LIDA) is a rare local complication of subcutaneous insulin application occurring in patients with diabetes type 1 and 2. A 45-year-old woman with an 11-year history of insulin-dependent diabetes mellitus type 1 underwent a mini-abdominoplasty and excision of a long-standing palpable mass in left hypogastric subcutaneous tissue in the area of long-term insulin application. Histopathological examination revealed insulin amyloidosis as a substrate of the mass lesion. Several months after surgery, there was a transient improvement in previously poor diabetes compensation. In addition to local allergic reactions, abscess formation, scarring, lipoatrophy/dystrophy, and lipohypertrophy, LIDA broadens the differential diagnostic spectrum of local insulin injection complications. LIDA has been described as a cause of poor glycemia compensation, probably due to the conversion of soluble insulin into insoluble amyloid fibrils, which prevents insulin from circulating in the blood and regulating glucose blood concentration. Improvement in diabetes compensation has been described in several reports, including our case. LIDA is a rare local complication of subcutaneous insulin application; accurate diagnosis and treatment have clinical consequences. Immunohistochemical or immunofluorescence distinction from other amyloid types is highly recommended. |
format | Online Article Text |
id | pubmed-10378134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103781342023-07-29 Localized Insulin-Derived Amyloidosis in Diabetes Mellitus Type 1 Patient: A Case Report Hrudka, Jan Sticová, Eva Krbcová, Magdaléna Schwarzmannová, Klára Diagnostics (Basel) Case Report Localized insulin-derived amyloidosis (LIDA) is a rare local complication of subcutaneous insulin application occurring in patients with diabetes type 1 and 2. A 45-year-old woman with an 11-year history of insulin-dependent diabetes mellitus type 1 underwent a mini-abdominoplasty and excision of a long-standing palpable mass in left hypogastric subcutaneous tissue in the area of long-term insulin application. Histopathological examination revealed insulin amyloidosis as a substrate of the mass lesion. Several months after surgery, there was a transient improvement in previously poor diabetes compensation. In addition to local allergic reactions, abscess formation, scarring, lipoatrophy/dystrophy, and lipohypertrophy, LIDA broadens the differential diagnostic spectrum of local insulin injection complications. LIDA has been described as a cause of poor glycemia compensation, probably due to the conversion of soluble insulin into insoluble amyloid fibrils, which prevents insulin from circulating in the blood and regulating glucose blood concentration. Improvement in diabetes compensation has been described in several reports, including our case. LIDA is a rare local complication of subcutaneous insulin application; accurate diagnosis and treatment have clinical consequences. Immunohistochemical or immunofluorescence distinction from other amyloid types is highly recommended. MDPI 2023-07-20 /pmc/articles/PMC10378134/ /pubmed/37510159 http://dx.doi.org/10.3390/diagnostics13142415 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Hrudka, Jan Sticová, Eva Krbcová, Magdaléna Schwarzmannová, Klára Localized Insulin-Derived Amyloidosis in Diabetes Mellitus Type 1 Patient: A Case Report |
title | Localized Insulin-Derived Amyloidosis in Diabetes Mellitus Type 1 Patient: A Case Report |
title_full | Localized Insulin-Derived Amyloidosis in Diabetes Mellitus Type 1 Patient: A Case Report |
title_fullStr | Localized Insulin-Derived Amyloidosis in Diabetes Mellitus Type 1 Patient: A Case Report |
title_full_unstemmed | Localized Insulin-Derived Amyloidosis in Diabetes Mellitus Type 1 Patient: A Case Report |
title_short | Localized Insulin-Derived Amyloidosis in Diabetes Mellitus Type 1 Patient: A Case Report |
title_sort | localized insulin-derived amyloidosis in diabetes mellitus type 1 patient: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378134/ https://www.ncbi.nlm.nih.gov/pubmed/37510159 http://dx.doi.org/10.3390/diagnostics13142415 |
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