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3,496 Possible Causes for Basal Cell Carcinoma, Relative Macrocephaly in Childhood, Rhabdomyosarcoma

  • Gorlin Syndrome

    […] syndrome (disorder) Naevoid basal cell carcinoma syndrome basal cell nevus syndrome Gorlin syndrome edit English nevoid basal cell carcinoma syndrome an autosomal dominant[] […] with NBCCS childhood medulloblastoma macrocephaly (occipital frontal circumference 97th centile) cleft lip/palate vertebral/rib anomalies preaxial or postaxial polydactyly[] Gorlin syndrome with synchronous rhabdomyosarcoma and Wilms tumor.[]

  • Prostate Rhabdomyosarcoma

    cell carcinoma Basal cell adenoma Basal cell carcinoma Urothelial carcinoma Prostatic stromal tumor of uncertain malignant potential Prostatic stromal sarcoma Atypical glands[] A biopsy of the prostate revealed embryonal rhabdomyosarcoma.[] Embryonal rhabdomyosarcoma of the prostate is typically a rare mesenchymal tumor of young boys, presenting with obstructive urinary symptoms or an abdominal mass.[]

    Missing: Relative Macrocephaly in Childhood
  • Orbital Neoplasm

    Studies show that basal cell carcinoma (BCC), retinoblastoma (RB), malignant melanoma, squamous cell carcinoma of the conjunctiva, and rhabdomyosarcoma are the most common[] الصفحة 136 - Radiation therapy for rhabdomyosarcoma: local failure risk for Clinical Group III patients on Intergroup Rhabdomyosarcoma Study II.[] With improvement in the therapeutic response or in the actual survival rates of children with such lesions as Wilms' tumour, brain tumours, rhabdomyosarcomas, Ewing's sarcoma[]

    Missing: Relative Macrocephaly in Childhood
  • Neurofibromatosis Type 1

    Gorlin Syndrome (nevoid basal cell carcinoma syndrome) Risk of developing cancerous and noncancerous tumors, most often basal cell carcinoma, less often meduloblastoma during[] The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[] Herein we present a rare combination of NF-1 and biliary rhabdomyosarcoma in a male infant.[]

  • Rhinophyma

    Basal cell carcinoma (BCC) is a rare finding in patients with rhinophyma.[] What is rhabdomyosarcoma? Rhabdomyosarcoma is a type of cancerous tumor that arises in the soft tissue, such as muscles.[] Previously, basal-cell carcinoma (BCC) has been reported in association with rhinophyma.[]

    Missing: Relative Macrocephaly in Childhood
  • Orbital Rhabdomyosarcoma

    Nevoid basal cell carcinoma (Gorlin) syndrome. Genet Med 2004;6:530-9. Sobel R, Woerner S. Rubinstein-Taybi Syndrome and nasopharyngeal rhabdomyosarcoma.[] Rhabdomyosarcoma is the most common primary orbital malignant tumor in children. Orbital lesions represent about 10 % of all the cases of rhabdomyosarcoma.[] Orbital rhabdomyosarcomas (ORM) are tumors of mesenchymal tissue and are primarily detected in the pediatric population.[]

    Missing: Relative Macrocephaly in Childhood
  • Rhabdomyosarcoma

    This article presents the case of a child presenting with a rhabdomyosarcoma associated with a fetal rhabdomyoma in the setting of nevoid basal cell carcinoma syndrome.[] Anne's page on rhabdomyosarcoma resources. Some of the links are outdated. Rhabdomyosarcoma at the Vanderbilt Medical Center site. Description of rhabdomyosarcoma at St.[] There is an increased risk in patients with certain genetic disorders - eg, Li-Fraumeni syndrome, neurofibromatosis, fetal alcohol syndrome and nevoid basal cell carcinoma[]

    Missing: Relative Macrocephaly in Childhood
  • Embryonal Rhabdomyosarcoma

    The spectrum of tumors found in Gorlin Syndrome includes basal cell carcinoma, medulloblastoma, and rarely, rhabdomyosarcoma (RMS).[] Embryonal rhabdomyosarcoma is the most common variant of the rare soft-tissue tumor, rhabdomyosarcomas, comprising up to 80% of it.[] cell carcinoma syndrome (NBCCS) (germline mutations in the hedgehog receptor PTCH gene) ( 16294371, 12204003 ) neurofibromatosis type 1 (NF1) ( 16434322 ) Associations ovarian[]

    Missing: Relative Macrocephaly in Childhood
  • Phakomatosis Pigmentokeratotica

    Pagina 369 - Nevoid basal cell carcinoma syndrome in a person with dark skin. J Am Acad Dermatol 2003; 49: 332-5 LeSueur BW, Silvis NG, Hansen RC.[] 1 Phacomatosis pigmentokeratotica: a case of HRAS mosaicism causing rhabdomyosarcoma. ( 29430633 ) 2018 2 Phacomatosis pigmentokeratotica and precocious puberty associated[] […] pigmentokeratotica: Postzygotic HRAS mutation with malignant degeneration of the sebaceous naevus. ( 30767209 ) 2019 2 Phacomatosis pigmentokeratotica: a case of HRAS mosaicism causing rhabdomyosarcoma[]

    Missing: Relative Macrocephaly in Childhood
  • Basal Cell Carcinoma of the Vulva

    Abstract A clinical and histopathologic study of material from a series of 17 patients with basal cell carcinoma of the vulva are reviewed.[] They include leiomyosarcomas, rhabdomyosarcomas, angiosarcomas, neurofibrosarcomas and epithelioid sarcomas.[] London, Royal College of Obstetricians and Gynaecologists Haroun SA, Elnaiem EA, Zaki MS, Adam I (2007) Aggressive rhabdomyosarcoma of the vulva in a young Sudanese woman.[]

    Missing: Relative Macrocephaly in Childhood

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