Renal Epithelioid Angiomyolipoma in Children
Renal angiomyolipoma is a rare cause of renal tumor in children. Most are associated with tuberous sclerosis, and the classic type is observed more commonly. Epithelioid angiomyolipoma is even rarer with only limited case reports and series published in literature, most of which are of adult patien...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Codon Publications
2021-06-01
|
Series: | Journal of Kidney Cancer and VHL |
Subjects: | |
Online Access: | http://www.jkcvhl.com/index.php/jkcvhl/article/view/178 |
id |
doaj-bdb8fc2b344c4305904a10f20e0a8288 |
---|---|
record_format |
Article |
spelling |
doaj-bdb8fc2b344c4305904a10f20e0a82882021-06-12T21:50:54ZengCodon PublicationsJournal of Kidney Cancer and VHL2203-58262021-06-018210.15586/jkcvhl.v8i2.178Renal Epithelioid Angiomyolipoma in ChildrenDhruv Mahajan0Vishesh Jain1Sandeep Agarwala2Manisha Jana3Prashant P Ramteke4All India Institute of Medical Sciences, Ansari Nagar, New Delhi, IndiaAll India Institute of Medical Sciences, New DelhiAll India Institute of Medical Sciences, New DelhiAll India Institute of Medical SciencesAll India Institute of Medical Sciences, New Delhi Renal angiomyolipoma is a rare cause of renal tumor in children. Most are associated with tuberous sclerosis, and the classic type is observed more commonly. Epithelioid angiomyolipoma is even rarer with only limited case reports and series published in literature, most of which are of adult patients. We describe a 12-year-old boy, a diagnosed patient of tuberous sclerosis, who presented with pain in the left flank. On evaluation, it was found to have a left renal mass with the clinical picture suggestive of renal cell carcinoma. Partial nephrectomy was performed and histopathology revealed epithelioid angiomyolipoma. The child was asymptomatic at follow-up after 3 months. Only a few such cases in children are found in literature, which are discussed alongside. Differential diagnosis of this rare tumor must be kept in mind in a renal tumor as surgery is generally curative in this possibly malignant tumor. Metastasis confers a poor prognosis. Chemotherapy is generally not effective, although various regimens have been tried. Tumor recurrence must be kept in mind and a follow-up after apparent complete remission is of paramount importance. http://www.jkcvhl.com/index.php/jkcvhl/article/view/178Angiomyolipoma; Kidney tumor; Pediatric cancer; Renal epithelioid angiomyolipoma; Tuberous sclerosis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Dhruv Mahajan Vishesh Jain Sandeep Agarwala Manisha Jana Prashant P Ramteke |
spellingShingle |
Dhruv Mahajan Vishesh Jain Sandeep Agarwala Manisha Jana Prashant P Ramteke Renal Epithelioid Angiomyolipoma in Children Journal of Kidney Cancer and VHL Angiomyolipoma; Kidney tumor; Pediatric cancer; Renal epithelioid angiomyolipoma; Tuberous sclerosis |
author_facet |
Dhruv Mahajan Vishesh Jain Sandeep Agarwala Manisha Jana Prashant P Ramteke |
author_sort |
Dhruv Mahajan |
title |
Renal Epithelioid Angiomyolipoma in Children |
title_short |
Renal Epithelioid Angiomyolipoma in Children |
title_full |
Renal Epithelioid Angiomyolipoma in Children |
title_fullStr |
Renal Epithelioid Angiomyolipoma in Children |
title_full_unstemmed |
Renal Epithelioid Angiomyolipoma in Children |
title_sort |
renal epithelioid angiomyolipoma in children |
publisher |
Codon Publications |
series |
Journal of Kidney Cancer and VHL |
issn |
2203-5826 |
publishDate |
2021-06-01 |
description |
Renal angiomyolipoma is a rare cause of renal tumor in children. Most are associated with tuberous sclerosis, and the classic type is observed more commonly. Epithelioid angiomyolipoma is even rarer with only limited case reports and series published in literature, most of which are of adult patients. We describe a 12-year-old boy, a diagnosed patient of tuberous sclerosis, who presented with pain in the left flank. On evaluation, it was found to have a left renal mass with the clinical picture suggestive of renal cell carcinoma. Partial nephrectomy was performed and histopathology revealed epithelioid angiomyolipoma. The child was asymptomatic at follow-up after 3 months. Only a few such cases in children are found in literature, which are discussed alongside. Differential diagnosis of this rare tumor must be kept in mind in a renal tumor as surgery is generally curative in this possibly malignant tumor. Metastasis confers a poor prognosis. Chemotherapy is generally not effective, although various regimens have been tried. Tumor recurrence must be kept in mind and a follow-up after apparent complete remission is of paramount importance.
|
topic |
Angiomyolipoma; Kidney tumor; Pediatric cancer; Renal epithelioid angiomyolipoma; Tuberous sclerosis |
url |
http://www.jkcvhl.com/index.php/jkcvhl/article/view/178 |
work_keys_str_mv |
AT dhruvmahajan renalepithelioidangiomyolipomainchildren AT visheshjain renalepithelioidangiomyolipomainchildren AT sandeepagarwala renalepithelioidangiomyolipomainchildren AT manishajana renalepithelioidangiomyolipomainchildren AT prashantpramteke renalepithelioidangiomyolipomainchildren |
_version_ |
1721380751993208832 |