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2,143 Possible Causes for DBP RB

Did you mean: DBP, RB

  • Malignant Neoplasm

    CONCLUSION: Retinoblastoma was most common solid malignant tumour in early age group.[] Abstract A case is reported about a patient who was originally treated for bilateral retinoblastoma and subsequently developed an embryonal rhabdomyosarcoma in the masseter[] OBJECTIVES: To report a case of a child with the hereditary form of unilateral retinoblastoma (RB), who developed Ewing's sarcoma of the right fibula 3 years after the enucleation[]

  • Visceral Larva Migrans

    These lesions, because they resemble retinoblastoma, have in the past led to unnecessary enucleation of the eye.[] […] detachment, inflammation of the eye tissues, retinal granulomas , and strabismus . [2] [8] [10] [11] Ocular granulomas resulting from OLM are frequently misdiagnosed as retinoblastomas[] Enucleation for suspected retinoblastoma, therefore, should not be performed without due consideration of the possibility of a benign granuloma caused by T. canis.[]

  • Osteosarcoma

    Li-Fraumeni syndrome, retinoblastoma, Rothmund-Thompson syndrome (type 2), Werner syndrome, and Bloom syndrome, constitute the majority of the tumor syndromes predisposing[] Children with an inherited form of retinoblastoma are more likely to develop osteosarcoma.[] Those include retinoblastoma, a rare eye cancer; Li-Fraumeni syndrome; Rothmund-Thompson syndrome; Diamond-Blackfan anemia; Bloom syndrome; and Werner syndrome.[]

  • Orbital Neoplasm

    Retinoblastoma: review of current management Oncologist 2007; 12: 1237-46. ].[] […] 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, retinoblastoma[] In 2002 about 2,300 primary eye tumors will be diagnosed in the United states, 75% of which will be choroidal melanomas, 20% retinoblastomas, and the remainder a wide variety[]

  • Rhabdomyosarcoma

    Second primary rhabdomyosarcomas in patients with bilateral retinoblastoma: a clinicopathologic and immunohistochemical study.[] Inherited retinoblastoma causes a kind of childhood eye cancer, but it can also increase the risk of other soft tissue sarcomas.[] TBX2 is also associated with two well-known cancer modifiers, the retinoblastoma tumour suppressor protein (pRB) and the Myc family.[]

  • Neurosyphilis

    The twentieth century was marked with frequent advances in the treatment and diagnosis of neurosyphilis. Once considered one of the most serious human diseases, neurosyphilis was paramount to a death sentence often preceded by agonizing pain and/or diminishing mental capacities. Since the introduction of[…][]

  • Testicular Germ Cell Tumor

    The retinoblastoma protein expression was determined using an antibody to retinoblastoma protein, Ser795.[] The expressions of gankyrin, retinoblastoma and retinoblastoma protein were analyzed in 93 testicular germ cell tumor samples and five normal human testis by immunohistochemistry[] OBJECTIVE: The oncoprotein, gankyrin, is known to facilitate cell proliferation through phosphorylation and degradation of retinoblastoma protein.[]

  • Waardenburg Syndrome

    CONCLUSION: We believe that this is the first description of a patient with retinoblastoma and Waardenburg syndrome and of an ovarian metastasis from retinoblastoma.[] RESULTS: Exploratory laparotomy revealed a right ovarian mass, and the excised ovary showed metastatic retinoblastoma.[] METHODS: Unilateral retinoblastoma was diagnosed in a 3-year-old girl with Waardenburg syndrome and leukocoria in the right eye.[]

  • Lipoma

    One patient with multiple ACL had a history of retinoblastoma.[] In the light of the available literature on adipocytic neoplasms in retinoblastoma survivors ( 30 patients with multiple lipomas following retinoblastoma reported), it is[] […] probably that retinoblastoma-associated lipomas belong to the ACL category.[]

  • Polydactyly

    CONCLUSIONS: Postaxial polydactyly should be considered as an association of retinoblastoma.[] BACKGROUND: Retinoblastoma is the most common primary intraocular malignancy of childhood, arising from retinal progenitor cells.[] The unusual associations reported with retinoblastoma are well-differentiated liposarcoma and lipomatous tissues, chromosome breakage syndromes, and the myriad findings of[]

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