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Right adrenal gland neuroblastoma infiltrating the liver and mimicking mesenchymal hamartoma: A case report
INTRODUCTION: Neuroblastoma is the most common extracranial solid pediatric malignancy. The most common site is abdomen with predominance of suprarenal medulla. Infiltration of the tumour to the liver is rare. No cases were reported in the literature about the misdiagnosis of neuroblastoma as mesenc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486106/ https://www.ncbi.nlm.nih.gov/pubmed/26036461 http://dx.doi.org/10.1016/j.ijscr.2015.05.024 |
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author | Abo-Elenain, Ahmed Naiem, Yousif Hamedhosam-eldin@hotmail.com, Hosam Emam, Mohamed Elkashef, Wagdi AbdelRafee, Ahmed |
author_facet | Abo-Elenain, Ahmed Naiem, Yousif Hamedhosam-eldin@hotmail.com, Hosam Emam, Mohamed Elkashef, Wagdi AbdelRafee, Ahmed |
author_sort | Abo-Elenain, Ahmed |
collection | PubMed |
description | INTRODUCTION: Neuroblastoma is the most common extracranial solid pediatric malignancy. The most common site is abdomen with predominance of suprarenal medulla. Infiltration of the tumour to the liver is rare. No cases were reported in the literature about the misdiagnosis of neuroblastoma as mesenchymal hamartoma in the liver. PRESENTATION OF CASE: We represent a rare case of neuroblastoma misdiagnosed as mesenchymal hamartoma in liver in a six-month-old female infant presented with fever and abdominal mass. Abdominal computed tomography (CT) revealed large cystic lesion occupying most of the right liver enchroaching upon right suprarenal region and displacing the right kidney inferior suggestive for mesenchymal hamartoma. Right adrenalectomy with en-bloc resection of the adjacent liver segments was done. Postoperative pathology revealed neuroblastoma with positive specific immunohistochemistry (IHC). DISCUSSION: Although neuroblastoma is the second most common pediatric abdominal malignancy with specific diagnostic modalities, a misdiagnosis of a case with neuroblastoma as mesenchymal hamartoma is rare. Histopathological diagnosis of neuroblastoma with positive IHC is essential as shown in our case. CONCLUSION: We represent a rare case of neuroblastoma which arose from the right adrenal gland and infiltrated the adjacent liver substance mimicking mesenchymal hamartoma of the liver. Neuroblastoma is rarely presented with pyrexia of unknown origin. Neuroblastoma should be considered in differential diagnosis of abdominal mass in all infants and children. |
format | Online Article Text |
id | pubmed-4486106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-44861062015-07-06 Right adrenal gland neuroblastoma infiltrating the liver and mimicking mesenchymal hamartoma: A case report Abo-Elenain, Ahmed Naiem, Yousif Hamedhosam-eldin@hotmail.com, Hosam Emam, Mohamed Elkashef, Wagdi AbdelRafee, Ahmed Int J Surg Case Rep Case Report INTRODUCTION: Neuroblastoma is the most common extracranial solid pediatric malignancy. The most common site is abdomen with predominance of suprarenal medulla. Infiltration of the tumour to the liver is rare. No cases were reported in the literature about the misdiagnosis of neuroblastoma as mesenchymal hamartoma in the liver. PRESENTATION OF CASE: We represent a rare case of neuroblastoma misdiagnosed as mesenchymal hamartoma in liver in a six-month-old female infant presented with fever and abdominal mass. Abdominal computed tomography (CT) revealed large cystic lesion occupying most of the right liver enchroaching upon right suprarenal region and displacing the right kidney inferior suggestive for mesenchymal hamartoma. Right adrenalectomy with en-bloc resection of the adjacent liver segments was done. Postoperative pathology revealed neuroblastoma with positive specific immunohistochemistry (IHC). DISCUSSION: Although neuroblastoma is the second most common pediatric abdominal malignancy with specific diagnostic modalities, a misdiagnosis of a case with neuroblastoma as mesenchymal hamartoma is rare. Histopathological diagnosis of neuroblastoma with positive IHC is essential as shown in our case. CONCLUSION: We represent a rare case of neuroblastoma which arose from the right adrenal gland and infiltrated the adjacent liver substance mimicking mesenchymal hamartoma of the liver. Neuroblastoma is rarely presented with pyrexia of unknown origin. Neuroblastoma should be considered in differential diagnosis of abdominal mass in all infants and children. Elsevier 2015-05-22 /pmc/articles/PMC4486106/ /pubmed/26036461 http://dx.doi.org/10.1016/j.ijscr.2015.05.024 Text en © 2015 The Authors http://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 Abo-Elenain, Ahmed Naiem, Yousif Hamedhosam-eldin@hotmail.com, Hosam Emam, Mohamed Elkashef, Wagdi AbdelRafee, Ahmed Right adrenal gland neuroblastoma infiltrating the liver and mimicking mesenchymal hamartoma: A case report |
title | Right adrenal gland neuroblastoma infiltrating the liver and mimicking mesenchymal hamartoma: A case report |
title_full | Right adrenal gland neuroblastoma infiltrating the liver and mimicking mesenchymal hamartoma: A case report |
title_fullStr | Right adrenal gland neuroblastoma infiltrating the liver and mimicking mesenchymal hamartoma: A case report |
title_full_unstemmed | Right adrenal gland neuroblastoma infiltrating the liver and mimicking mesenchymal hamartoma: A case report |
title_short | Right adrenal gland neuroblastoma infiltrating the liver and mimicking mesenchymal hamartoma: A case report |
title_sort | right adrenal gland neuroblastoma infiltrating the liver and mimicking mesenchymal hamartoma: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486106/ https://www.ncbi.nlm.nih.gov/pubmed/26036461 http://dx.doi.org/10.1016/j.ijscr.2015.05.024 |
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