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A Case of Small Intestinal Ileus Due to Wandering Spleen with a Large Cyst
Patient: Female, 28 Final Diagnosis: Ileus due to wandering spleen with a cyst Symptoms: Acute abdominal pain Medication: — Clinical Procedure: Tube decompression • laparotomy Specialty: Abdominal Surgery • Transplant Surgery OBJECTIVE: Rare disease BACKGROUND: Splenic cysts are rare. Most are due t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Scientific Literature, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690211/ https://www.ncbi.nlm.nih.gov/pubmed/31371695 http://dx.doi.org/10.12659/AJCR.916845 |
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author | Matsuyama, Takehisa Nakao, Toshimasa Harada, Shumpei Nakamura, Tsukasa Nobori, Shuji Ushigome, Hidetaka |
author_facet | Matsuyama, Takehisa Nakao, Toshimasa Harada, Shumpei Nakamura, Tsukasa Nobori, Shuji Ushigome, Hidetaka |
author_sort | Matsuyama, Takehisa |
collection | PubMed |
description | Patient: Female, 28 Final Diagnosis: Ileus due to wandering spleen with a cyst Symptoms: Acute abdominal pain Medication: — Clinical Procedure: Tube decompression • laparotomy Specialty: Abdominal Surgery • Transplant Surgery OBJECTIVE: Rare disease BACKGROUND: Splenic cysts are rare. Most are due to previous trauma, infection, or infarction. They are generally handled by laparoscopic surgical removal if they are larger than 5 cm. However, very large cysts may require splenectomy. Another factor in the choice of therapy is the patient’s underlying condition. We present the case of a giant splenic cyst in a woman 1 year after a renal transplant. CASE REPORT: A 28-year-old woman presented with acute abdominal pain and nausea. One year before, she had received an ABO-identical living donor renal transplantation from her father, and was maintained on oral tacrolimus and prednisolone. A CT scan with contrast showed enteric ileus and an abnormal position of the spleen, which was involved by a cyst measuring 12×12.5×9 cm. A nasogastric tube, and later a small bowel tube, were inserted to decompress the ileus. The patient underwent laparotomy 11 days after admission. We confirmed an internal hernia with volvulus due to migration of the spleen; however, there was no evidence of necrosis. The patient was treated with splenectomy and reduction of the hernia. There were no complications. CONCLUSIONS: This was a very unusual emergency following renal transplantation. Splenectomy has been performed in the past for immunosuppression in cases of donor ABO-incompatibility. We therefore considered that it would be more expedient to remove the spleen than to remove the cyst and perform splenopexy. |
format | Online Article Text |
id | pubmed-6690211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66902112019-08-28 A Case of Small Intestinal Ileus Due to Wandering Spleen with a Large Cyst Matsuyama, Takehisa Nakao, Toshimasa Harada, Shumpei Nakamura, Tsukasa Nobori, Shuji Ushigome, Hidetaka Am J Case Rep Articles Patient: Female, 28 Final Diagnosis: Ileus due to wandering spleen with a cyst Symptoms: Acute abdominal pain Medication: — Clinical Procedure: Tube decompression • laparotomy Specialty: Abdominal Surgery • Transplant Surgery OBJECTIVE: Rare disease BACKGROUND: Splenic cysts are rare. Most are due to previous trauma, infection, or infarction. They are generally handled by laparoscopic surgical removal if they are larger than 5 cm. However, very large cysts may require splenectomy. Another factor in the choice of therapy is the patient’s underlying condition. We present the case of a giant splenic cyst in a woman 1 year after a renal transplant. CASE REPORT: A 28-year-old woman presented with acute abdominal pain and nausea. One year before, she had received an ABO-identical living donor renal transplantation from her father, and was maintained on oral tacrolimus and prednisolone. A CT scan with contrast showed enteric ileus and an abnormal position of the spleen, which was involved by a cyst measuring 12×12.5×9 cm. A nasogastric tube, and later a small bowel tube, were inserted to decompress the ileus. The patient underwent laparotomy 11 days after admission. We confirmed an internal hernia with volvulus due to migration of the spleen; however, there was no evidence of necrosis. The patient was treated with splenectomy and reduction of the hernia. There were no complications. CONCLUSIONS: This was a very unusual emergency following renal transplantation. Splenectomy has been performed in the past for immunosuppression in cases of donor ABO-incompatibility. We therefore considered that it would be more expedient to remove the spleen than to remove the cyst and perform splenopexy. International Scientific Literature, Inc. 2019-08-02 /pmc/articles/PMC6690211/ /pubmed/31371695 http://dx.doi.org/10.12659/AJCR.916845 Text en © Am J Case Rep, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Articles Matsuyama, Takehisa Nakao, Toshimasa Harada, Shumpei Nakamura, Tsukasa Nobori, Shuji Ushigome, Hidetaka A Case of Small Intestinal Ileus Due to Wandering Spleen with a Large Cyst |
title | A Case of Small Intestinal Ileus Due to Wandering Spleen with a Large Cyst |
title_full | A Case of Small Intestinal Ileus Due to Wandering Spleen with a Large Cyst |
title_fullStr | A Case of Small Intestinal Ileus Due to Wandering Spleen with a Large Cyst |
title_full_unstemmed | A Case of Small Intestinal Ileus Due to Wandering Spleen with a Large Cyst |
title_short | A Case of Small Intestinal Ileus Due to Wandering Spleen with a Large Cyst |
title_sort | case of small intestinal ileus due to wandering spleen with a large cyst |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690211/ https://www.ncbi.nlm.nih.gov/pubmed/31371695 http://dx.doi.org/10.12659/AJCR.916845 |
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