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Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report
INTRODUCTION AND IMPORTANCE: Childhood colorectal cancers are extremely rare and so is Osteochondromatosis. Both diseases do not have epidemiological records in African countries. The aim of this report is to present a rare coexistence of CRC and multiple enchondromas in a child. PRESENTATION OF CAS...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382775/ https://www.ncbi.nlm.nih.gov/pubmed/37354823 http://dx.doi.org/10.1016/j.ijscr.2023.108427 |
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author | Ramírez Calas, Ramon Andres González Millán, Tania Mohammed, Sheriff Azahares Leal, German Amadu, Munira Sadat Seidu, Anwar |
author_facet | Ramírez Calas, Ramon Andres González Millán, Tania Mohammed, Sheriff Azahares Leal, German Amadu, Munira Sadat Seidu, Anwar |
author_sort | Ramírez Calas, Ramon Andres |
collection | PubMed |
description | INTRODUCTION AND IMPORTANCE: Childhood colorectal cancers are extremely rare and so is Osteochondromatosis. Both diseases do not have epidemiological records in African countries. The aim of this report is to present a rare coexistence of CRC and multiple enchondromas in a child. PRESENTATION OF CASE: A case of a 12-year-old boy who presented with a large bowel obstruction secondary to an advanced tumor of the descending colon. He was also diagnosed with multiple osteochondromas affecting legs, arms, ribs, scapula, clavicle and pelvis. No positive family history was recorded. An urgent left hemicolectomy and diverting transverse colostomy was done. The colon can as stage IIIB and the patient received adjuvant chemotherapy. After 8 months of follow up, the colostomy was successfully reversed without any endoscopic signs of tumor growth or distant metastasis. CLINICAL DISCUSSION: Colorectal cancer in childhood is rare. It may present with aggressive histological subtypes in children as compared to adults. There is little to no reports on the coexistence of colorectal cancer and multiple Osteochondromatosis. Microsatellite instability in DNA tumor is common in Colon Cancer and variety of mutations of EXT-1 and EXT-2 genes goes with Enchondromatosis. CONCLUSION: The coexistence of two rare conditions is the remarkable issue in this case report. There are no prior reports in literature. Further genomic sequencing maybe required to better understand this coexistence. |
format | Online Article Text |
id | pubmed-10382775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103827752023-07-30 Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report Ramírez Calas, Ramon Andres González Millán, Tania Mohammed, Sheriff Azahares Leal, German Amadu, Munira Sadat Seidu, Anwar Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Childhood colorectal cancers are extremely rare and so is Osteochondromatosis. Both diseases do not have epidemiological records in African countries. The aim of this report is to present a rare coexistence of CRC and multiple enchondromas in a child. PRESENTATION OF CASE: A case of a 12-year-old boy who presented with a large bowel obstruction secondary to an advanced tumor of the descending colon. He was also diagnosed with multiple osteochondromas affecting legs, arms, ribs, scapula, clavicle and pelvis. No positive family history was recorded. An urgent left hemicolectomy and diverting transverse colostomy was done. The colon can as stage IIIB and the patient received adjuvant chemotherapy. After 8 months of follow up, the colostomy was successfully reversed without any endoscopic signs of tumor growth or distant metastasis. CLINICAL DISCUSSION: Colorectal cancer in childhood is rare. It may present with aggressive histological subtypes in children as compared to adults. There is little to no reports on the coexistence of colorectal cancer and multiple Osteochondromatosis. Microsatellite instability in DNA tumor is common in Colon Cancer and variety of mutations of EXT-1 and EXT-2 genes goes with Enchondromatosis. CONCLUSION: The coexistence of two rare conditions is the remarkable issue in this case report. There are no prior reports in literature. Further genomic sequencing maybe required to better understand this coexistence. Elsevier 2023-06-21 /pmc/articles/PMC10382775/ /pubmed/37354823 http://dx.doi.org/10.1016/j.ijscr.2023.108427 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Ramírez Calas, Ramon Andres González Millán, Tania Mohammed, Sheriff Azahares Leal, German Amadu, Munira Sadat Seidu, Anwar Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report |
title | Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report |
title_full | Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report |
title_fullStr | Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report |
title_full_unstemmed | Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report |
title_short | Advanced colon cancer coexisting with multiple Osteochondromatosis in a child; coincidence or causality? - A case report |
title_sort | advanced colon cancer coexisting with multiple osteochondromatosis in a child; coincidence or causality? - a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382775/ https://www.ncbi.nlm.nih.gov/pubmed/37354823 http://dx.doi.org/10.1016/j.ijscr.2023.108427 |
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