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  1. AU="Kan, Amanda N C"
  2. AU="Lan, Ching-Yu"
  3. AU="Dietrich, Fine"
  4. AU="de Araujo, Cristiano-Miranda"

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  1. Artikel ; Online: Kaposiform haemangioendothelioma of the spine associated with fixed hyperlordotic deformity and Kasabach-Merritt Syndrome: a case report and literature review.

    Chin, Leanne H Q / Fung, Kevin K F / Chan, Joyce P K / Kan, Amanda N C / Yuen, M K

    Skeletal radiology

    2022  Band 52, Heft 4, Seite(n) 783–790

    Abstract: Kaposiform haemangioendothelioma (KHE) is a rare childhood disease classified by the International Society for the Study of Vascular Anomalies (ISSVA) as a locally aggressive vascular tumor. It has been reported to affect any site, with a predilection ... ...

    Abstract Kaposiform haemangioendothelioma (KHE) is a rare childhood disease classified by the International Society for the Study of Vascular Anomalies (ISSVA) as a locally aggressive vascular tumor. It has been reported to affect any site, with a predilection for the extremities and trunk. Although it typically manifests as an enlarging cutaneous or soft tissue lesion, less than 10% of cases have no skin involvement, with the retroperitoneum being the most frequently involved extracutaneous site. Approximately twenty cases of KHE with bony involvement have been reported in the literature to date, with only five of those cases involving the spine specifically.We present a, rare case of KHE who presented with progressive fixed hyperlordotic deformity, multiple non-specific spinal lesions, and abnormal blood tests, posing a clinical and radiological diagnostic challenge. Additionally, we conducted a thorough review of the literature to compare and contrast the various multimodality imaging manifestations of KHE involving the spine.
    Mesh-Begriff(e) Humans ; Child ; Kasabach-Merritt Syndrome/diagnostic imaging ; Kasabach-Merritt Syndrome/complications ; Hemangioendothelioma/complications ; Hemangioendothelioma/diagnostic imaging ; Sarcoma, Kaposi/complications ; Sarcoma, Kaposi/diagnosis ; Sarcoma, Kaposi/pathology ; Vascular Neoplasms ; Lordosis
    Sprache Englisch
    Erscheinungsdatum 2022-08-10
    Erscheinungsland Germany
    Dokumenttyp Review ; Case Reports ; Journal Article
    ZDB-ID 527592-1
    ISSN 1432-2161 ; 0364-2348
    ISSN (online) 1432-2161
    ISSN 0364-2348
    DOI 10.1007/s00256-022-04152-z
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Durable disease control with apatinib, irinotecan and temozolomide in a case of metastatic primitive myxoid mesenchymal tumour of infancy.

    Yu, S H / Kan, Amanda N C / To, K F / Lam, Y L / Yan, Carol L S / Liu, Anthony P Y / Ku, Dennis T L

    Pediatric blood & cancer

    2022  Band 70, Heft 3, Seite(n) e30026

    Mesh-Begriff(e) Humans ; Infant ; Irinotecan ; Temozolomide ; Neoplasms ; Pyridines
    Chemische Substanzen Irinotecan (7673326042) ; apatinib (5S371K6132) ; Temozolomide (YF1K15M17Y) ; Pyridines
    Sprache Englisch
    Erscheinungsdatum 2022-11-28
    Erscheinungsland United States
    Dokumenttyp Case Reports ; Letter
    ZDB-ID 2131448-2
    ISSN 1545-5017 ; 1545-5009
    ISSN (online) 1545-5017
    ISSN 1545-5009
    DOI 10.1002/pbc.30026
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel: Case Report: Primary Thoracic Low-Grade Fibromyxoid Sarcoma in a Young Girl Presenting With Mediastinal Mass Syndrome.

    Chan, Yat Chi / Kan, Amanda N C / Yuen, Liz Y P / Wan, Innes Y P / Fung, Kevin K F / Cheung, Yiu-Fai / Leung, Karen K Y / Ku, Dennis T L / Liu, Anthony P Y

    Frontiers in pediatrics

    2022  Band 10, Seite(n) 885068

    Abstract: Low-grade fibromyxoid sarcomas (LGFMSs) are typically adult-onset tumors that arise from the extremities. Here, we report an exceptional case of primary thoracic LGFMS in an 8-year-old girl that resulted in mediastinal syndrome. In reporting this case, ... ...

    Abstract Low-grade fibromyxoid sarcomas (LGFMSs) are typically adult-onset tumors that arise from the extremities. Here, we report an exceptional case of primary thoracic LGFMS in an 8-year-old girl that resulted in mediastinal syndrome. In reporting this case, we discuss the clinical challenges, role of molecular profiling and review reported cases of pediatric thoracic LGFMSs.
    Sprache Englisch
    Erscheinungsdatum 2022-06-17
    Erscheinungsland Switzerland
    Dokumenttyp Case Reports
    ZDB-ID 2711999-3
    ISSN 2296-2360
    ISSN 2296-2360
    DOI 10.3389/fped.2022.885068
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel: Patterns of care and survival of Chinese glioblastoma patients in the temozolomide era: a Hong Kong population-level analysis over a 14-year period.

    Woo, Peter Y M / Yau, Stephen / Lam, Tai-Chung / Pu, Jenny K S / Li, Lai-Fung / Lui, Louisa C Y / Chan, Danny T M / Loong, Herbert H F / Lee, Michael W Y / Yeung, Rebecca / Kwok, Carol C H / Au, Siu-Kie / Tan, Tze-Ching / Kan, Amanda N C / Chan, Tony K T / Mak, Calvin H K / Mak, Henry K F / Ho, Jason M K / Cheung, Ka-Man /
    Tse, Teresa P K / Lau, Sarah S N / Chow, Joyce S W / El-Helali, Aya / Ng, Ho-Keung / Poon, Wai-Sang

    Neuro-oncology practice

    2022  Band 10, Heft 1, Seite(n) 50–61

    Abstract: Background: The aim of this study is to address the paucity of epidemiological data regarding the characteristics, treatment patterns and survival outcomes of Chinese glioblastoma patients.: Methods: This was a population-level study of Hong Kong ... ...

    Abstract Background: The aim of this study is to address the paucity of epidemiological data regarding the characteristics, treatment patterns and survival outcomes of Chinese glioblastoma patients.
    Methods: This was a population-level study of Hong Kong adult (
    Results: One thousand and ten patients with a median follow-up of 10.0 months were reviewed. The ASIR of glioblastoma was 1.0 per 100 000 population with no significant change during the study period. The mean age was 57
    Conclusions: The incidence of glioblastoma in the Chinese general population is low. We charted the development of neuro-oncological care of glioblastoma patients in Hong Kong during the temozolomide era. Although there was an increased adoption of temozolomide chemoradiotherapy, a corresponding improvement in survival was not observed.
    Sprache Englisch
    Erscheinungsdatum 2022-09-10
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 2768945-1
    ISSN 2054-2585 ; 2054-2577
    ISSN (online) 2054-2585
    ISSN 2054-2577
    DOI 10.1093/nop/npac069
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Endoplasmic reticulum chaperone prolyl 4-hydroxylase, beta polypeptide (P4HB) promotes malignant phenotypes in glioma via MAPK signaling.

    Sun, Stella / Kiang, Karrie M Y / Ho, Amy S W / Lee, Derek / Poon, Ming-Wai / Xu, Fei-Fan / Pu, Jenny K S / Kan, Amanda N C / Lee, Nikki P Y / Liu, Xiao-Bing / Man, Kwan / Day, Philip J R / Lui, Wai-Man / Fung, Ching-Fai / Leung, Gilberto K K

    Oncotarget

    2017  Band 8, Heft 42, Seite(n) 71911–71923

    Abstract: Endoplasmic reticulum (ER) chaperone Prolyl 4-hydroxylase, beta polypeptide (P4HB) has previously been identified as a novel target for chemoresistance in glioblastoma multiforme (GBM). Yet its functional roles in glioma carcinogenesis remain elusive. In ...

    Abstract Endoplasmic reticulum (ER) chaperone Prolyl 4-hydroxylase, beta polypeptide (P4HB) has previously been identified as a novel target for chemoresistance in glioblastoma multiforme (GBM). Yet its functional roles in glioma carcinogenesis remain elusive. In clinical analysis using human glioma specimens and Gene Expression Omnibus (GEO) profiles, we found that aberrant expression of P4HB was correlated with high-grade malignancy and an angiogenic phenotype in glioma. Furthermore, P4HB upregulation conferred malignant characteristics including proliferation, invasion, migration and angiogenesis
    Sprache Englisch
    Erscheinungsdatum 2017-09-22
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2560162-3
    ISSN 1949-2553 ; 1949-2553
    ISSN (online) 1949-2553
    ISSN 1949-2553
    DOI 10.18632/oncotarget.18026
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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