[PDF] Top 20 Urachal Tumor: A Case Report of an Extremely Rare Carcinoma

... Urachus carcinoma is a rare entity, with quite limited pub- lished ...first case report in ...(a) tumor in the dome of the bladder, (b) absence of cystitis cystica and ... See full document

... revealed an epithelial syringomatous population, while HMB45 positivity in the melanocytic population confirmed the presence of a melanoma in situ, thus drawing a clear boundary be- tween the two ... See full document

... lesions of the oral cavity are extremely rare, accounting for approximately 1% of all malignant oral ...sources of metastatic tumors in the oral region are, from the most to the least ... See full document

... a rare type of breast cancer and are presented as a heterogeneous group of lesions with different histological types, such as, ductal carcinoma in situ arising in an intraductal ... See full document

... excision of the lesion with skin grafting was carried out ...cycles of chemotherapy and ...complaint of a firm mass (1.5 cm) on the right side of his frontal region which had appeared since 2 ... See full document

... neuroectodermal tumor of infancy (MNTI) is a rare neoplasm that affects mainly children under 1 year of ...evaluation of a lesion with 1 month of ...underwent an ... See full document

... is an embryological remnant of urogenital sinus and allantois that usually involutes before birth and remains as the median umbilical ...Pathogenesis of urachal carcinoma is not fully ... See full document

... is an infectious disease caused by ...5% of all echinococcal infections in endemic areas, and is almost always secondary to the hepatic or pulmonary ...hydatidosis of cervicofacial region is ... See full document

... Metastatic tumor accounts for 3 – 7% of orbital neoplasm and any part of the orbit may be involved ...primary tumor are carcinoma of the breast and lung ...Hepatocellular ... See full document

... first report of a case of coexisting benign phyllodes tumor and invasive ductal carcinoma in distinct ...association of carcin- oma and phyllodes in situ tumor is ... See full document

... common tumor found in patients with chronic temporal lobe ...agenesis of the corpus callosum. Rarely hypervascularized, the presence of intratumoral bleeding is not common and, in the majority ... See full document

... outcome of the disease, there are reports of patients with FIGO stages II to IV having a lower probability of long-term survival than patients with stage-I ...Age, tumor size, clinical stage, ... See full document

... is an analysis and a study on the Solitary Fibrous Tumor of the Pleura (SFTP), which is a neoplasm of origin in the pluripotent cells of the fibrous ...a rare tumor type ... See full document

... Ewing's tumor is an aggressive bone neoplasm that representatives approximately 6% of primary bone ...decade of life, with a mild predominance in men and rare in black ...group ... See full document

... that of colorectal ...intestine, an adenoma- carcinoma sequence is assumed to occur in the appendix as ...70% of cases and Loss of Heterozygosity (LOH) at 5q22, 6q, 17p13, and 18q21 are ... See full document

... hyperaemia, an elevated choroidal mass lesion of size 3DD was seen in the superotemporal quadrant with surrounding exudative retinal detachment ...was an elevated mass lesion of 3DD size in ... See full document

... because of her general ...score of 50 on the Karnofsky performance scale (KPS). An MRI scan (Figure 1) performed on the patient a few days before this evaluation was brought with her and this showed ... See full document

... Cell Carcinoma (TCC), or renal Urothelial Carcinoma (UC), is a malignant tumor arising from the transitional (urothelial) epithelial cells lining the urinary tract from the renal calyces to the ... See full document

... are rare, painful, and benign soft tissue tumors of the skin arising from the glomus body, an arteriovenous thermoregulatory ...Glomus tumor involving the external genital organs including ... See full document

... this report, we describe a young male patient with an enlarging soft tissue mass in his second left maxillary molar socket that resemble any benign soft tissue mass in the absence neurofibromatosis type I ... See full document