Create issue ticket

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[wikidata.org] […] with NBCCS childhood medulloblastoma macrocephaly (occipital frontal circumference 97th centile) cleft lip/palate vertebral/rib anomalies preaxial or postaxial polydactyly[invitae.com] Gorlin syndrome with synchronous rhabdomyosarcoma and Wilms tumor.[ncbi.nlm.nih.gov]

  • Prostate Rhabdomyosarcoma

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

    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[benthamopen.com] الصفحة 136 - Radiation therapy for rhabdomyosarcoma: local failure risk for Clinical Group III patients on Intergroup Rhabdomyosarcoma Study II.[books.google.com] 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[books.google.com]

    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[doi.org] The number of café au lait macules increases with age in childhood, similar to what is observed in NF1 [Author, personal observation]. Macrocephaly.[web.archive.org] Herein we present a rare combination of NF-1 and biliary rhabdomyosarcoma in a male infant.[ncbi.nlm.nih.gov]

  • Rhinophyma

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

    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.[eyewiki.aao.org] Rhabdomyosarcoma is the most common primary orbital malignant tumor in children. Orbital lesions represent about 10 % of all the cases of rhabdomyosarcoma.[ncbi.nlm.nih.gov] Orbital rhabdomyosarcomas (ORM) are tumors of mesenchymal tissue and are primarily detected in the pediatric population.[symptoma.com]

    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.[ncbi.nlm.nih.gov] Anne's page on rhabdomyosarcoma resources. Some of the links are outdated. Rhabdomyosarcoma at the Vanderbilt Medical Center site. Description of rhabdomyosarcoma at St.[web.archive.org] There is an increased risk in patients with certain genetic disorders - eg, Li-Fraumeni syndrome, neurofibromatosis, fetal alcohol syndrome and nevoid basal cell carcinoma[patient.info]

    Missing: Relative Macrocephaly in Childhood
  • Embryonal Rhabdomyosarcoma

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

    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.[books.google.ro] 1 Phacomatosis pigmentokeratotica: a case of HRAS mosaicism causing rhabdomyosarcoma. ( 29430633 ) 2018 2 Phacomatosis pigmentokeratotica and precocious puberty associated[malacards.org] […] pigmentokeratotica: Postzygotic HRAS mutation with malignant degeneration of the sebaceous naevus. ( 30767209 ) 2019 2 Phacomatosis pigmentokeratotica: a case of HRAS mosaicism causing rhabdomyosarcoma[malacards.org]

    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.[ncbi.nlm.nih.gov] They include leiomyosarcomas, rhabdomyosarcomas, angiosarcomas, neurofibrosarcomas and epithelioid sarcomas.[cancerresearchuk.org] 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.[omicsonline.org]

    Missing: Relative Macrocephaly in Childhood

Similar symptoms