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A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma
Acquired hemophilia A (AHA) is a rare disease that results from factor VIII inhibitors causing abnormal coagulation, and certain cases may develop after highly invasive surgery. The present case study reports on a 68-year-old male patient who developed AHA after undergoing a subtotal stomach-preserv...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442756/ https://www.ncbi.nlm.nih.gov/pubmed/37614988 http://dx.doi.org/10.3892/br.2023.1643 |
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author | Takahashi, Makoto Morita, Yasuhiro Hayashi, Tatsuya Higashihara, Taku Kawasaki, Keishi Sato, Shunsuke Yokose, Shota Sasaki, Shu Funakoshi, Kaoruko Sasaki, Takayoshi Zhou, Daren Ichinose, Akinori Ohtsuka, Hideo Ishibasi, Yuji Hatao, Fumihiko Shimizu, Keiki Isono, Nobuo Sasaki, Naomi Kozai, Yasuji Okada, Haruka Chikasawa, Yushi |
author_facet | Takahashi, Makoto Morita, Yasuhiro Hayashi, Tatsuya Higashihara, Taku Kawasaki, Keishi Sato, Shunsuke Yokose, Shota Sasaki, Shu Funakoshi, Kaoruko Sasaki, Takayoshi Zhou, Daren Ichinose, Akinori Ohtsuka, Hideo Ishibasi, Yuji Hatao, Fumihiko Shimizu, Keiki Isono, Nobuo Sasaki, Naomi Kozai, Yasuji Okada, Haruka Chikasawa, Yushi |
author_sort | Takahashi, Makoto |
collection | PubMed |
description | Acquired hemophilia A (AHA) is a rare disease that results from factor VIII inhibitors causing abnormal coagulation, and certain cases may develop after highly invasive surgery. The present case study reports on a 68-year-old male patient who developed AHA after undergoing a subtotal stomach-preserving pancreatoduodenectomy for distal cholangiocarcinoma. The patient experienced complications after surgery, requiring reoperation on postoperative day (PD) 5 due to rupture of the Braun's enterostomy. On PD 6, angiography was performed after bleeding was detected in the jejunal limb, but hemostasis occurred spontaneously during the examination. Bleeding was observed again on PD 8 and direct surgical ligation was performed. On PD 14, bleeding recurred in the jejunal limb and angiography was performed to embolize the periphery of the second jejunal artery. During the procedure, the prothrombin time was normal, but only the activated partial thromboplastin time was prolonged. A close examination of the coagulation system revealed a decrease in factor VIII levels and the presence of factor VIII inhibitors, resulting in the diagnosis of AHA. Administration of steroids was initiated on PD 15 and, in addition to daily blood transfusions, activated prothrombin complex concentrate was administered to achieve hemostasis. The patient was discharged from the intensive care unit on PD 36 but later developed an intractable labial fistula due to suture failure at the gastrojejunostomy site. As the use of factor VIII inhibitors continued despite the administration of steroids, cyclophosphamide (CPA) pulse therapy was added at PD 58. However, CPA was ineffective and the administration of rituximab was initiated on PD 98. After 12 courses of rituximab, the patient tested negative for factor VIII inhibitors on PD 219. On PD 289, labial fistula closure was performed with continuous replacement of factor VIII and the patient was discharged on PD 342. |
format | Online Article Text |
id | pubmed-10442756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-104427562023-08-23 A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma Takahashi, Makoto Morita, Yasuhiro Hayashi, Tatsuya Higashihara, Taku Kawasaki, Keishi Sato, Shunsuke Yokose, Shota Sasaki, Shu Funakoshi, Kaoruko Sasaki, Takayoshi Zhou, Daren Ichinose, Akinori Ohtsuka, Hideo Ishibasi, Yuji Hatao, Fumihiko Shimizu, Keiki Isono, Nobuo Sasaki, Naomi Kozai, Yasuji Okada, Haruka Chikasawa, Yushi Biomed Rep Articles Acquired hemophilia A (AHA) is a rare disease that results from factor VIII inhibitors causing abnormal coagulation, and certain cases may develop after highly invasive surgery. The present case study reports on a 68-year-old male patient who developed AHA after undergoing a subtotal stomach-preserving pancreatoduodenectomy for distal cholangiocarcinoma. The patient experienced complications after surgery, requiring reoperation on postoperative day (PD) 5 due to rupture of the Braun's enterostomy. On PD 6, angiography was performed after bleeding was detected in the jejunal limb, but hemostasis occurred spontaneously during the examination. Bleeding was observed again on PD 8 and direct surgical ligation was performed. On PD 14, bleeding recurred in the jejunal limb and angiography was performed to embolize the periphery of the second jejunal artery. During the procedure, the prothrombin time was normal, but only the activated partial thromboplastin time was prolonged. A close examination of the coagulation system revealed a decrease in factor VIII levels and the presence of factor VIII inhibitors, resulting in the diagnosis of AHA. Administration of steroids was initiated on PD 15 and, in addition to daily blood transfusions, activated prothrombin complex concentrate was administered to achieve hemostasis. The patient was discharged from the intensive care unit on PD 36 but later developed an intractable labial fistula due to suture failure at the gastrojejunostomy site. As the use of factor VIII inhibitors continued despite the administration of steroids, cyclophosphamide (CPA) pulse therapy was added at PD 58. However, CPA was ineffective and the administration of rituximab was initiated on PD 98. After 12 courses of rituximab, the patient tested negative for factor VIII inhibitors on PD 219. On PD 289, labial fistula closure was performed with continuous replacement of factor VIII and the patient was discharged on PD 342. D.A. Spandidos 2023-08-01 /pmc/articles/PMC10442756/ /pubmed/37614988 http://dx.doi.org/10.3892/br.2023.1643 Text en Copyright: © Takahashi et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Takahashi, Makoto Morita, Yasuhiro Hayashi, Tatsuya Higashihara, Taku Kawasaki, Keishi Sato, Shunsuke Yokose, Shota Sasaki, Shu Funakoshi, Kaoruko Sasaki, Takayoshi Zhou, Daren Ichinose, Akinori Ohtsuka, Hideo Ishibasi, Yuji Hatao, Fumihiko Shimizu, Keiki Isono, Nobuo Sasaki, Naomi Kozai, Yasuji Okada, Haruka Chikasawa, Yushi A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma |
title | A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma |
title_full | A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma |
title_fullStr | A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma |
title_full_unstemmed | A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma |
title_short | A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma |
title_sort | case of acquired hemophilia a after pancreaticoduodenectomy for distal cholangiocarcinoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442756/ https://www.ncbi.nlm.nih.gov/pubmed/37614988 http://dx.doi.org/10.3892/br.2023.1643 |
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