نتایج جستجو برای: neuroectodermal tumor
تعداد نتایج: 430331 فیلتر نتایج به سال:
primitive neuroectodermal tumor (pnet) of kidney is an extremely rare renal neoplasm with only about fifty reported cases in literature. presumably,of neural crest origin, these tumors behave aggressively and carry a poor prognosis. we report a case of 22-year old female patient complaining of left loin pain with recurrent hematuria for last 3 months. on clinical exam...
conclusions pnet/ews should be included in the differential diagnosis of renal tumors in symptomatic young adults. patients with localised pnet/ews treated with a combination of surgery and chemotherapy have an excellent chance of long-term survival, as in the case we have presented. introduction primitive neuroectodermal tumor (pnet)/ewing’s sarcoma (ews) belongs to a family of neoplasms that ...
primitive neuroectodermal tumor (penets) is an uncommon malignancy of bone and soft tissue witch rarely occurs in the kidney. in more than 90% of the cases, the tumor cells relieves a balanced translocation (11; 22) (q24; q12). immunohistochemical staining may be required for diagnosis of penet. the cells of tumor express cd99, vimentin, nse, fl1 but do not express ck, lca, myogenin, and wt1. w...
Primary intraspinal primitive neuroectodermal tumor (PNET) is a type of round cell malignant which reported only above 100 in literature. We report case Dorsal Spine Primitive Neuroectodermal Tumor (P.N.E.T) Presenting with Features Pott’s Spine, & discuss its pathological features, radiology, and treatment options.
Background and Objectives: Melanotic neuroectodermal tumor of infancy (MNTI) is a rare, usually benign neoplasm of neural crest origin. MNTI usually arises in infants within the first year of life. The tumor is usually observed in head and neck areas especially in maxilla; however it has been reported in other areas such as hip, bone marrow, and ovary as well. It usually appears as a ...
background: we report the analgesic efficacy of lumbar epidural adenosine injection in reducing the chronic neuropathic pain in a patient with primitive neuroectodermal tumor. report of the case: in this case report a 13-year-old male with primary neuroectodermal tumor (pnet) was administered in epidural space with adenosine to reduce his pain. the patient received 10ml of 0.25% ropivacaine and...
this is the report of a mandibular neuroectodermal/ewing sarcoma in an 8-year-old male cross breed dogthat is unique because of tumor origin location. pedunculated, ulcerative, firm 6.0 × 4.0 × 5.5 cm tumor masseffaced the bone at the rostral part of the mandible and had a white-sanguineous color at cross sectionappearance. histopathologically, small round blue cell tumor was diagnosed. immunoh...
Peripheral primitive neuroectodermal tumor (pPNET) is a highly aggressive small round cell tumor belonging to PNET/Ewing sarcoma family. Ovarian tumors composed of primitive neuroectodermal elements are extremely rare. Herein we reported two cases of peripheral primitive neuroectodermal tumors of ovary in two patients with different clinical presentations. Definite diagnoses were made bas...
ewing’s sarcoma is a round cell malignancy of bone and soft tissue that occurs predominately in adolescents and young adults.it is an uncommon malignancy, but is recognized as the second most prevalent primary bone tumor worldwide. extraosseous ewing’s sarcoma is extremely rare and can affect the skin, soft tissues, or viscera. prognostic and therapeutic features of ewing’s extraosseous tumors ...
The primitive neuroectodermal tumor (PNET) belongs to a group of highly malignant tumors and is composed of small round cells of a neuroectodermal origin. Categorized in the same tumor family as Ewing sarcoma, the PNET is most likely to occur in bones and soft tissues. However, a small number of PNET cases arising in the pelvis have been reported as well. We present three cases of pelvic PNET: ...
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