Cargando…
Pseudo-wound infection after a caesarean section: Case report of unrecognized Pyoderma Gangrenosum
BACKGROUND: Pyoderma Gangrenosum (PG) is a rare auto-inflammatory disease, characterized by painful ulcerative skin-lesions often developing at sites of injury or surgery because of the typical pathergy phenomena. We describe an unusual case of PG after a caesarean section with excessive extra-cutan...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171254/ https://www.ncbi.nlm.nih.gov/pubmed/32305662 http://dx.doi.org/10.1016/j.ijscr.2020.03.041 |
_version_ | 1783524034662629376 |
---|---|
author | van Donkelaar, Carlina E. de Haan, Johanna M.H. Lange, Johan F.M. de Vries, Marjolijn Horváth, Barbara |
author_facet | van Donkelaar, Carlina E. de Haan, Johanna M.H. Lange, Johan F.M. de Vries, Marjolijn Horváth, Barbara |
author_sort | van Donkelaar, Carlina E. |
collection | PubMed |
description | BACKGROUND: Pyoderma Gangrenosum (PG) is a rare auto-inflammatory disease, characterized by painful ulcerative skin-lesions often developing at sites of injury or surgery because of the typical pathergy phenomena. We describe an unusual case of PG after a caesarean section with excessive extra-cutaneous manifestation within internal organs. PRESENTATION OF CASE: A 21-year-old Dutch primigravida developed signs of sepsis after a caesarean section. Despite antibiotic treatment, fast clinical deterioration occurred. Exploration of the wound showed necrosis of the uterus and surrounding tissues. Due to the progression of necrosis, consecutive debridement procedures were executed resulting in a substantial abdominal wall defect. The progressive clinical course of the necrosis combined with absence of positive wound cultures and histology of prominent interstitial neutrophilic infiltration, led to the diagnosis ‘Pyoderma Gangrenosum’. Treatment with high dose corticosteroids led to rapid regression of the disease. After several weeks, the abdominal wall defect was surgically corrected under systemic corticosteroid therapy. DISCUSSION: This case of PG is unique due to the excessive extra-cutaneous presentation, which contributed to delayed diagnosis. Several surgical interventions in the active stage of disease resulted in expansion of PG and substantial morbidity for the patient. CONCLUSION: Post-operative PG can mimic infectious diseases, but treatment is substantially different. This case of extensive PG highlights the importance of timely recognition and treatment of the disease to reduce iatrogenic morbidity. |
format | Online Article Text |
id | pubmed-7171254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-71712542020-04-22 Pseudo-wound infection after a caesarean section: Case report of unrecognized Pyoderma Gangrenosum van Donkelaar, Carlina E. de Haan, Johanna M.H. Lange, Johan F.M. de Vries, Marjolijn Horváth, Barbara Int J Surg Case Rep Article BACKGROUND: Pyoderma Gangrenosum (PG) is a rare auto-inflammatory disease, characterized by painful ulcerative skin-lesions often developing at sites of injury or surgery because of the typical pathergy phenomena. We describe an unusual case of PG after a caesarean section with excessive extra-cutaneous manifestation within internal organs. PRESENTATION OF CASE: A 21-year-old Dutch primigravida developed signs of sepsis after a caesarean section. Despite antibiotic treatment, fast clinical deterioration occurred. Exploration of the wound showed necrosis of the uterus and surrounding tissues. Due to the progression of necrosis, consecutive debridement procedures were executed resulting in a substantial abdominal wall defect. The progressive clinical course of the necrosis combined with absence of positive wound cultures and histology of prominent interstitial neutrophilic infiltration, led to the diagnosis ‘Pyoderma Gangrenosum’. Treatment with high dose corticosteroids led to rapid regression of the disease. After several weeks, the abdominal wall defect was surgically corrected under systemic corticosteroid therapy. DISCUSSION: This case of PG is unique due to the excessive extra-cutaneous presentation, which contributed to delayed diagnosis. Several surgical interventions in the active stage of disease resulted in expansion of PG and substantial morbidity for the patient. CONCLUSION: Post-operative PG can mimic infectious diseases, but treatment is substantially different. This case of extensive PG highlights the importance of timely recognition and treatment of the disease to reduce iatrogenic morbidity. Elsevier 2020-04-13 /pmc/articles/PMC7171254/ /pubmed/32305662 http://dx.doi.org/10.1016/j.ijscr.2020.03.041 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article van Donkelaar, Carlina E. de Haan, Johanna M.H. Lange, Johan F.M. de Vries, Marjolijn Horváth, Barbara Pseudo-wound infection after a caesarean section: Case report of unrecognized Pyoderma Gangrenosum |
title | Pseudo-wound infection after a caesarean section: Case report of unrecognized Pyoderma Gangrenosum |
title_full | Pseudo-wound infection after a caesarean section: Case report of unrecognized Pyoderma Gangrenosum |
title_fullStr | Pseudo-wound infection after a caesarean section: Case report of unrecognized Pyoderma Gangrenosum |
title_full_unstemmed | Pseudo-wound infection after a caesarean section: Case report of unrecognized Pyoderma Gangrenosum |
title_short | Pseudo-wound infection after a caesarean section: Case report of unrecognized Pyoderma Gangrenosum |
title_sort | pseudo-wound infection after a caesarean section: case report of unrecognized pyoderma gangrenosum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171254/ https://www.ncbi.nlm.nih.gov/pubmed/32305662 http://dx.doi.org/10.1016/j.ijscr.2020.03.041 |
work_keys_str_mv | AT vandonkelaarcarlinae pseudowoundinfectionafteracaesareansectioncasereportofunrecognizedpyodermagangrenosum AT dehaanjohannamh pseudowoundinfectionafteracaesareansectioncasereportofunrecognizedpyodermagangrenosum AT langejohanfm pseudowoundinfectionafteracaesareansectioncasereportofunrecognizedpyodermagangrenosum AT devriesmarjolijn pseudowoundinfectionafteracaesareansectioncasereportofunrecognizedpyodermagangrenosum AT horvathbarbara pseudowoundinfectionafteracaesareansectioncasereportofunrecognizedpyodermagangrenosum |