Primary epithelioid rhabdomyosarcoma of the stomach: a case report and review of literature

Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual case of primary epithelioid rhabdomyosarcoma of the stomach and review the literature. A 64-year-old woman presented with a lesion at the gastroesopha...

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Published inDiagnostic pathology Vol. 14; no. 1; p. 137
Main Authors Wang, Yangkun, Guo, Pei, Zhang, Zhishang, Jiang, Runde, Li, Zuguo
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 23.12.2019
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Abstract Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual case of primary epithelioid rhabdomyosarcoma of the stomach and review the literature. A 64-year-old woman presented with a lesion at the gastroesophageal junction. Histopathological examination showed irregularly sized round cells with low cytoplasmic content and eccentric nuclei. Mitotic figures were present. Fibrovascular septa and areas of necrosis were observed between tumor cells. Tumor cells were strongly positive for MyoD1, desmin, and myogenin, and weakly positive for actin, CD56, and PGP9.5. The ki-67 index was ≥90%. Primary epithelioid rhabdomyosarcoma of the stomach is extremely rare. Better awareness of this entity is necessary for early diagnosis and treatment.
AbstractList Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual case of primary epithelioid rhabdomyosarcoma of the stomach and review the literature. A 64-year-old woman presented with a lesion at the gastroesophageal junction. Histopathological examination showed irregularly sized round cells with low cytoplasmic content and eccentric nuclei. Mitotic figures were present. Fibrovascular septa and areas of necrosis were observed between tumor cells. Tumor cells were strongly positive for MyoD1, desmin, and myogenin, and weakly positive for actin, CD56, and PGP9.5. The ki-67 index was ≥90%. Primary epithelioid rhabdomyosarcoma of the stomach is extremely rare. Better awareness of this entity is necessary for early diagnosis and treatment.
Background Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual case of primary epithelioid rhabdomyosarcoma of the stomach and review the literature. Case presentation A 64-year-old woman presented with a lesion at the gastroesophageal junction. Histopathological examination showed irregularly sized round cells with low cytoplasmic content and eccentric nuclei. Mitotic figures were present. Fibrovascular septa and areas of necrosis were observed between tumor cells. Tumor cells were strongly positive for MyoD1, desmin, and myogenin, and weakly positive for actin, CD56, and PGP9.5. The ki-67 index was ≥90%. Conclusions Primary epithelioid rhabdomyosarcoma of the stomach is extremely rare. Better awareness of this entity is necessary for early diagnosis and treatment.
Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual case of primary epithelioid rhabdomyosarcoma of the stomach and review the literature. Primary epithelioid rhabdomyosarcoma of the stomach is extremely rare. Better awareness of this entity is necessary for early diagnosis and treatment.
Background Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual case of primary epithelioid rhabdomyosarcoma of the stomach and review the literature. Case presentation A 64-year-old woman presented with a lesion at the gastroesophageal junction. Histopathological examination showed irregularly sized round cells with low cytoplasmic content and eccentric nuclei. Mitotic figures were present. Fibrovascular septa and areas of necrosis were observed between tumor cells. Tumor cells were strongly positive for MyoD1, desmin, and myogenin, and weakly positive for actin, CD56, and PGP9.5. The ki-67 index was [greater than or equai to]90%. Conclusions Primary epithelioid rhabdomyosarcoma of the stomach is extremely rare. Better awareness of this entity is necessary for early diagnosis and treatment. Keywords: Gastric tumor, Epithelioid rhabdomyosarcoma, Clinicopathological features, Immunohistochemistry
Abstract Background Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual case of primary epithelioid rhabdomyosarcoma of the stomach and review the literature. Case presentation A 64-year-old woman presented with a lesion at the gastroesophageal junction. Histopathological examination showed irregularly sized round cells with low cytoplasmic content and eccentric nuclei. Mitotic figures were present. Fibrovascular septa and areas of necrosis were observed between tumor cells. Tumor cells were strongly positive for MyoD1, desmin, and myogenin, and weakly positive for actin, CD56, and PGP9.5. The ki-67 index was ≥90%. Conclusions Primary epithelioid rhabdomyosarcoma of the stomach is extremely rare. Better awareness of this entity is necessary for early diagnosis and treatment.
BACKGROUNDEpithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual case of primary epithelioid rhabdomyosarcoma of the stomach and review the literature.CASE PRESENTATIONA 64-year-old woman presented with a lesion at the gastroesophageal junction. Histopathological examination showed irregularly sized round cells with low cytoplasmic content and eccentric nuclei. Mitotic figures were present. Fibrovascular septa and areas of necrosis were observed between tumor cells. Tumor cells were strongly positive for MyoD1, desmin, and myogenin, and weakly positive for actin, CD56, and PGP9.5. The ki-67 index was ≥90%.CONCLUSIONSPrimary epithelioid rhabdomyosarcoma of the stomach is extremely rare. Better awareness of this entity is necessary for early diagnosis and treatment.
Abstract Background Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual case of primary epithelioid rhabdomyosarcoma of the stomach and review the literature. Case presentation A 64-year-old woman presented with a lesion at the gastroesophageal junction. Histopathological examination showed irregularly sized round cells with low cytoplasmic content and eccentric nuclei. Mitotic figures were present. Fibrovascular septa and areas of necrosis were observed between tumor cells. Tumor cells were strongly positive for MyoD1, desmin, and myogenin, and weakly positive for actin, CD56, and PGP9.5. The ki-67 index was ≥90%. Conclusions Primary epithelioid rhabdomyosarcoma of the stomach is extremely rare. Better awareness of this entity is necessary for early diagnosis and treatment.
ArticleNumber 137
Audience Academic
Author Li, Zuguo
Wang, Yangkun
Guo, Pei
Jiang, Runde
Zhang, Zhishang
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Cites_doi 10.1309/AJCPRQES4NFDQ0XC
10.1016/j.soc.2016.05.001
10.1016/j.ejso.2018.07.058
10.3748/wjg.v21.i15.4680
10.1097/PAT.0000000000000321
10.4103/IJPM.IJPM_785_17
10.1159/000449126
10.1007/s12029-012-9379-0
10.1182/blood-2016-04-712109
10.5858/arpa.2014-0475-OA
10.1111/cup.12340
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Issue 1
Keywords Immunohistochemistry
Clinicopathological features
Epithelioid rhabdomyosarcoma
Gastric tumor
Language English
License Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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References SN Bowe (917_CR5) 2011; 136
Y-K Wang (917_CR12) 2002; 31
P Agarwal (917_CR4) 2018; 61
A van der Veen (917_CR10) 2018; 44
PC Feasel (917_CR6) 2014; 41
JS Gandhi (917_CR9) 2012; 43
Y-K Wang (917_CR11) 2015; 21
GO Hofmann (917_CR14) 1990; 61
M Iwamuro (917_CR18) 2018; 2018
M Palermo (917_CR8) 2012; 42
917_CR13
917_CR15
J Wang (917_CR2) 2013; 42
L Yu (917_CR7) 2015; 47
VY Jo (917_CR1) 2016; 25
ER Rudzinski (917_CR3) 2015; 139
917_CR16
S Khuri (917_CR17) 2016; 9
A Schmitt-Graeff (917_CR19) 2016; 128
References_xml – volume: 136
  start-page: 587
  issue: 4
  year: 2011
  ident: 917_CR5
  publication-title: Am J Clin Pathol
  doi: 10.1309/AJCPRQES4NFDQ0XC
  contributor:
    fullname: SN Bowe
– volume: 25
  start-page: 621
  issue: 4
  year: 2016
  ident: 917_CR1
  publication-title: Surg Oncol Clin N Am
  doi: 10.1016/j.soc.2016.05.001
  contributor:
    fullname: VY Jo
– volume: 44
  start-page: 155
  issue: 12
  year: 2018
  ident: 917_CR10
  publication-title: Eur J Surg Oncol
  doi: 10.1016/j.ejso.2018.07.058
  contributor:
    fullname: A van der Veen
– volume: 21
  start-page: 4680
  issue: 15
  year: 2015
  ident: 917_CR11
  publication-title: World J Gastroenterol
  doi: 10.3748/wjg.v21.i15.4680
  contributor:
    fullname: Y-K Wang
– volume: 31
  start-page: 151
  issue: 2
  year: 2002
  ident: 917_CR12
  publication-title: Chin J Pathol
  contributor:
    fullname: Y-K Wang
– volume: 47
  start-page: 667
  issue: 7
  year: 2015
  ident: 917_CR7
  publication-title: Pathology
  doi: 10.1097/PAT.0000000000000321
  contributor:
    fullname: L Yu
– volume: 61
  start-page: 77
  issue: 1
  year: 1990
  ident: 917_CR14
  publication-title: Chirurg
  contributor:
    fullname: GO Hofmann
– volume: 42
  start-page: 363
  issue: 6
  year: 2013
  ident: 917_CR2
  publication-title: Zhonghua Bing Li Xue Za Zhi
  contributor:
    fullname: J Wang
– volume: 61
  start-page: 258
  issue: 2
  year: 2018
  ident: 917_CR4
  publication-title: Indian J Pathol Microbiol
  doi: 10.4103/IJPM.IJPM_785_17
  contributor:
    fullname: P Agarwal
– ident: 917_CR15
– volume: 9
  start-page: 666
  issue: 3
  year: 2016
  ident: 917_CR17
  publication-title: Case Rep Oncol
  doi: 10.1159/000449126
  contributor:
    fullname: S Khuri
– volume: 42
  start-page: 131
  issue: 2
  year: 2012
  ident: 917_CR8
  publication-title: Case report Acta Gastroenterol Latinoam
  contributor:
    fullname: M Palermo
– volume: 43
  start-page: S217
  issue: Suppl 1
  year: 2012
  ident: 917_CR9
  publication-title: J Gastrointest Cancer
  doi: 10.1007/s12029-012-9379-0
  contributor:
    fullname: JS Gandhi
– volume: 128
  start-page: 460
  issue: 3
  year: 2016
  ident: 917_CR19
  publication-title: Blood
  doi: 10.1182/blood-2016-04-712109
  contributor:
    fullname: A Schmitt-Graeff
– volume: 2018
  start-page: 8054284
  year: 2018
  ident: 917_CR18
  publication-title: Case Rep Gastrointest Med
  contributor:
    fullname: M Iwamuro
– ident: 917_CR16
– ident: 917_CR13
– volume: 139
  start-page: 1281
  issue: 10
  year: 2015
  ident: 917_CR3
  publication-title: Arch Pathol Lab Med
  doi: 10.5858/arpa.2014-0475-OA
  contributor:
    fullname: ER Rudzinski
– volume: 41
  start-page: 588
  issue: 7
  year: 2014
  ident: 917_CR6
  publication-title: J Cutan Pathol
  doi: 10.1111/cup.12340
  contributor:
    fullname: PC Feasel
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Snippet Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual case of...
Abstract Background Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe...
Background Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an...
BACKGROUNDEpithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe an unusual...
Abstract Background Epithelioid rhabdomyosarcoma is a rare tumor that generally occurs in the bladder, the parotid gland, or the skin of the neck. We describe...
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StartPage 137
SubjectTerms Actin
Age
Bladder
Case Report
Case reports
CD56 antigen
Clinicopathological features
Cytoplasm
Desmin
Epithelioid rhabdomyosarcoma
Gastric cancer
Gastric tumor
Gastrointestinal diseases
Immunohistochemistry
Literature reviews
Melanoma
Morphology
Muscle proteins
Myogenin
Necrosis
Parotid gland
Rhabdomyosarcoma
Septum
Skin
Skin cancer
Stomach
Tumor cells
Tumors
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Title Primary epithelioid rhabdomyosarcoma of the stomach: a case report and review of literature
URI https://www.ncbi.nlm.nih.gov/pubmed/31870387
https://www.proquest.com/docview/2340733634
https://search.proquest.com/docview/2330330474
https://pubmed.ncbi.nlm.nih.gov/PMC6929344
https://doaj.org/article/ce9e7ed37f0d44ee81128b4194622b81
Volume 14
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