Total: 32 |
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PMID (PMCID) | ||
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30582192 |
FEMALE | Middle Aged |
Neuroblastoma-like schwannoma with giant rosette: A potential diagnostic pitfall for hyalinizing spindle cell tumor. | ||
Koubaa Mahjoub W, Jouini R, Khanchel F, Ben Brahim E, Llamas-Velasco M, Helel I, Khayat O, Chadli A, Badri T, Mentzel T. J Cutan Pathol. 2019;46(3):234-237. |
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Neuroblastoma-like schwannoma with giant rosette: A potential diagnostic pitfall for hyalinizing spindle cell tumor. | ||
30582192 |
FEMALE | Middle Aged |
Neuroblastoma-like schwannoma with giant rosette: A potential diagnostic pitfall for hyalinizing spindle cell tumor. | ||
Koubaa Mahjoub W, Jouini R, Khanchel F, Ben Brahim E, Llamas-Velasco M, Helel I, Khayat O, Chadli A, Badri T, Mentzel T. J Cutan Pathol. 2019;46(3):234-237. |
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We propose the term "neuroblastoma-like schwannoma" when there are small rosettes, "HSCT-like schwannoma" for tumors with giant rosettes and "collagen-rich schwannoma" when there are "ill-defined" structures reminiscent of rosettes. | ||
30582192 |
FEMALE | Middle Aged |
Neuroblastoma-like schwannoma with giant rosette: A potential diagnostic pitfall for hyalinizing spindle cell tumor. | ||
Koubaa Mahjoub W, Jouini R, Khanchel F, Ben Brahim E, Llamas-Velasco M, Helel I, Khayat O, Chadli A, Badri T, Mentzel T. J Cutan Pathol. 2019;46(3):234-237. |
||
We propose the term "neuroblastoma-like schwannoma" when there are small rosettes, "HSCT-like schwannoma" for tumors with giant rosettes and "collagen-rich schwannoma" when there are "ill-defined" structures reminiscent of rosettes. | ||
30582192 |
FEMALE | Middle Aged |
Neuroblastoma-like schwannoma with giant rosette: A potential diagnostic pitfall for hyalinizing spindle cell tumor. | ||
Koubaa Mahjoub W, Jouini R, Khanchel F, Ben Brahim E, Llamas-Velasco M, Helel I, Khayat O, Chadli A, Badri T, Mentzel T. J Cutan Pathol. 2019;46(3):234-237. |
||
We propose the term "neuroblastoma-like schwannoma" when there are small rosettes, "HSCT-like schwannoma" for tumors with giant rosettes and "collagen-rich schwannoma" when there are "ill-defined" structures reminiscent of rosettes. | ||
29758594 |
MALE | Infant |
PHOX2B is a reliable immunomarker in distinguishing peripheral neuroblastic tumours from CNS embryonal tumours. | ||
Alexandrescu S, Paulson V, Dubuc A, Ligon A, Lidov HG. Histopathology. 2018;73(3):483-491. |
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PHOX2B immunostain was performed on 29 paediatric cases, with adequate controls: one retroperitoneal embryonal tumour in a child with retinoblastoma (index 1), one posterior fossa embryonal tumour in a child with a neuroblastoma (index 2), seven medulloblastomas, four atypical teratoid/rhabdoid tumours (ATRT), four retinoblastomas, six pineoblastomas, four embryonal tumours with multilayered rosettes (ETMR) and two CNS embryonal tumours, not elsewhere classified. | ||
26658063 |
MALE | Infant |
Embryonal Tumor With Abundant Neuropil and True Rosettes: A Distinct Immunohistochemical Pattern. | ||
Al-Salam S, Al Alashari M. Appl Immunohistochem Mol Morphol. 2016;24(6):e41-9. |
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Embryonal tumors with abundant neuropil and true rosettes (ETANTR) are rare pediatric embryonal neoplasms that combine features of neuroblastoma and ependymoblastoma. | ||
23865520 (3867594) |
FEMALE | |
The role of CD133+ cells in a recurrent embryonal tumor with abundant neuropil and true rosettes (ETANTR). | ||
Hervey-Jumper SL, Altshuler DB, Wang AC, He X, Maher CO, Robertson PL, Garton HJ, Fan X, Muraszko KM, Camelo-Piragua S. Brain Pathol. 2014;24(1):45-51. |
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Embryonal tumor with abundant neuropil and true rosettes (ETANTR) is a recently described embryonal neoplasm of the central nervous system, consisting of a well-circumscribed embryonal tumor of infancy with mixed features of ependymoblastoma (multilayer ependymoblastic rosettes and pseudorosettes) and neuroblastoma (neuroblastic rosettes) in the presence of neuropil-like islands. | ||
23865520 (3867594) |
FEMALE | |
The role of CD133+ cells in a recurrent embryonal tumor with abundant neuropil and true rosettes (ETANTR). | ||
Hervey-Jumper SL, Altshuler DB, Wang AC, He X, Maher CO, Robertson PL, Garton HJ, Fan X, Muraszko KM, Camelo-Piragua S. Brain Pathol. 2014;24(1):45-51. |
||
Embryonal tumor with abundant neuropil and true rosettes (ETANTR) is a recently described embryonal neoplasm of the central nervous system, consisting of a well-circumscribed embryonal tumor of infancy with mixed features of ependymoblastoma (multilayer ependymoblastic rosettes and pseudorosettes) and neuroblastoma (neuroblastic rosettes) in the presence of neuropil-like islands. | ||
23865520 (3867594) |
FEMALE | |
The role of CD133+ cells in a recurrent embryonal tumor with abundant neuropil and true rosettes (ETANTR). | ||
Hervey-Jumper SL, Altshuler DB, Wang AC, He X, Maher CO, Robertson PL, Garton HJ, Fan X, Muraszko KM, Camelo-Piragua S. Brain Pathol. 2014;24(1):45-51. |
||
Embryonal tumor with abundant neuropil and true rosettes (ETANTR) is a recently described embryonal neoplasm of the central nervous system, consisting of a well-circumscribed embryonal tumor of infancy with mixed features of ependymoblastoma (multilayer ependymoblastic rosettes and pseudorosettes) and neuroblastoma (neuroblastic rosettes) in the presence of neuropil-like islands. | ||
25208992 |
MIXED_SAMPLE | Infant |
[Primitive neuroectodermal tumor of central nervous system with features of ependymoblastoma and neuroblastoma: a clinicopathologic study of 4 cases]. | ||
Wang R, Guan W, Wu X, Zhang W, Jiang B, Ma J, Wang L. Zhonghua Bing Li Xue Za Zhi. 2014;43(6):403-7. |
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All tumors showed typical combined histological patterns of ependymoblastoma and neuroblastoma, demonstrating zones of true rosettes, occasional pseudovascular rosettes, and undifferentiated neuroepithelial cells in a prominent background of mature neuropils. | ||
25208992 |
MIXED_SAMPLE | Infant |
[Primitive neuroectodermal tumor of central nervous system with features of ependymoblastoma and neuroblastoma: a clinicopathologic study of 4 cases]. | ||
Wang R, Guan W, Wu X, Zhang W, Jiang B, Ma J, Wang L. Zhonghua Bing Li Xue Za Zhi. 2014;43(6):403-7. |
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All tumors showed typical combined histological patterns of ependymoblastoma and neuroblastoma, demonstrating zones of true rosettes, occasional pseudovascular rosettes, and undifferentiated neuroepithelial cells in a prominent background of mature neuropils. | ||
21194275 |
MALE | Infant |
Embryonal tumors with abundant neuropil and true rosettes: 2 illustrative cases and a review of the literature. | ||
Manjila S, Ray A, Hu Y, Cai DX, Cohen ML, Cohen AR. Neurosurg Focus. 2011;30(1):E2. |
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Histologically, this tumor has features of ependymoblastoma and neuroblastoma, demonstrating areas of fine fibrillary neuropil intermingled with ependymoblastic rosettes and zones of undifferentiated neuroepithelial cells. | ||
19922484 |
FEMALE | Adult |
Cutaneous neuroblastoma-like schwannoma: a report of two cases, one with a plexiform pattern, and a review of the literature. | ||
Suchak R, Luzar B, Bacchi CE, Maguire B, Calonje E. J Cutan Pathol. 2010;37(9):997-1001. |
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The differential diagnosis includes other lesions with the formation of rosettes including neuroblastoma, low-grade fibromyxoid sarcoma and dendritic cell neurofibroma, as well as primitive neuroectodermal tumors and rare malignant transformation in a schwannoma. | ||
20499240 |
FEMALE | Infant |
Embryonal tumor with abundant neuropil and true rosettes (ETANTR): a new distinctive variety of pediatric PNET: a case-based update. | ||
Ferri Niguez B, Martinez-Lage JF, Almagro MJ, Fuster JL, Serrano C, Torroba MA, Sola J. Childs Nerv Syst. 2010;26(8):1003-8. |
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ETANTR is a recently described variety of PNET that combines microscopic features of neuroblastoma and ependymoblastoma, demonstrating areas of fine fibrillary neuropil intermingled with cellular zones and ependymoblastic rosettes. | ||
17641710 |
MALE | |
Neuroblastoma-like schwannoma as a rare cause of proptosis: a case report. | ||
Kukreja M, Gupta R, Julka A, Sharma MC. Can J Ophthalmol. 2007;42(4):624-5. |
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Schwannoma with giant rosettes and hyperchromatic small cells was previously designated a neuroblastoma-like schwannoma by Goldblum et al. | ||
16919032 |
FEMALE | Adult |
Rosetoid schwannoma (neuroblastoma-like) in association with an anetoderma. | ||
Velez D, Reina Duran T, Perez-Gala S, Fernandez JF. J Cutan Pathol. 2006;33(8):573-6. |
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A cutaneous biopsy showed findings consistent with a neuroblastoma-like schwannoma with the following peculiar features: (i) Being fully composed of rosette-like structures. | ||
15900131 |
FEMALE | Adult |
Schwannoma with neuroblastoma-like rosettes: an unusual morphologic variant. | ||
Lewis ZT, Geisinger KR, Pichardo R, Sangueza OP. Am J Dermatopathol. 2005;27(3):243-6. |
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Schwannoma with neuroblastoma-like rosettes: an unusual morphologic variant. | ||
12544097 |
OTHER | Middle Aged |
Neuroblastoma-like schwannoma: a case report and review of the literature. | ||
de Saint Aubain Somerhausen N, Valaeys V, Geerts M, Andre J. Am J Dermatopathol. 2003;25(1):32-4. |
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Schwannoma with giant rosettes, previously designated as neuroblastoma-like schwannoma by Goldblum et al., must be differentiated from neuroblastoma, peripheral neuroectodermal tumors, and malignant change in a schwannoma. | ||
12544097 |
OTHER | Middle Aged |
Neuroblastoma-like schwannoma: a case report and review of the literature. | ||
de Saint Aubain Somerhausen N, Valaeys V, Geerts M, Andre J. Am J Dermatopathol. 2003;25(1):32-4. |
||
Schwannoma with giant rosettes, previously designated as neuroblastoma-like schwannoma by Goldblum et al., must be differentiated from neuroblastoma, peripheral neuroectodermal tumors, and malignant change in a schwannoma. | ||
11843557 |
FEMALE | Adult |
Fine needle aspiration cytology of metastatic olfactory neuroblastoma: a case report. | ||
Chung J, Park ST, Jang J. Acta Cytol. 2002;46(1):40-5. |
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ONB, like adrenal neuroblastoma, shows distinctive cytologic features, including a rosette or pseudorosette and fibrillary network. |