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Query: UMLS:C0027651 (tumor)
 685,946 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A 20-month-old boy with a ciliary body tumor presented with two white flocculi floating in the anterior chamber of his left eye. This material was examined by electron microscopy. Both the clinical appearance of the tumor and the ultrastructural findings suggested the diagnosis of medulloepithelioma. The flocculi contained tumor cells forming lumina and displaying neuronal-type cilia, neurotubules, and a complex band of apical desmonosomal junctions. Since the last finding is not present in retinoblastoma rosettes in the absence of fleurette differentiation, it distinguishes medulloepithelioma from retinoblastoma. The electron microscopic diagnosis has permitted a trial period of conservative cryotherapy directed at the tumor and the associated glaucoma. The electron microscopic characteristics of the tumor favor the neuroepitheliomatous and neuroblastic differentiation of medulloepithelioma rather than ependymal differentiation.
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PMID:Electron microscopic diagnosis of medulloepithelioma. 111

A direct causal relationship between a human DNA virus, adeno serotype 12, and malignant transformation in target cells (sensory retinal neuronal precursors) was suggested by the development of a remarkably uniform retinoblastoma-like neoplasm in rats. In order to focus upon incipient photoreceptor differentiation, 27 3-day-old CD rats were selected for intraocular virus inoculation. A single injection of 0.03 ml of the virus fluid, 104.5 TCID50 HeLa cells/0.1 ml was given in the left eye. Within 73 to 167 days after the virus inoculation, 12 rats (44.4%) developed retinal tumors in the left eye. Although retinal tumors mimicking human retinoblastoma with true rosettes were anticipated, the highly uniform histopathologic appearance of all 12 eyes was virtually indistinguishable from that of 0-day-old rats. However, multiple foci of malignant cells fusing with the inner segment of relatively well-differentiated retinal layers were found haphazardly throughout the cases; such retinal remnants were not detectable in tumors of 0-day-old rats. Electron microscopy revealed poorly differentiated tumor cells that possessed a single cilium consisting of a typical ring of nine doublets with no axial pair (a 9 plus 0 pattern). Advenovirus-specific T-antigens detected in vivo by the immunofluorescein microscopic procedure in abortively infected or transformed cells clearly indicated that some neuronal precursors destined for part of the ganglioneuronic layer are selectively susceptible to viral oncogenesis. No preferential involvement of the photoreceptor cells was observed. No control animals developed retinal neoplasms.
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PMID:Retinal tumor induction by ocular inoculation of human adneovirus in 3-day-old rats. 111 20

A number of human tumor cell lines of both neural and nonneural origin have been assayed for the expression of an interspecies brain antigen (mouse brain antigen 2), detected by naturally occurring antibodies in normal mouse sera. These experiments indicate that mouse brain antigen 2 is present on four human neuroblastoma cell lines but not on other human tumor cell lines tested, including four glial cell lines and a retinoblastoma. These findings demonstrate the value of naturally occurring antibodies in normal mouse sera for the detection and serological classification of human tumor antigens and indicate that considerable caution should be used in attempts to distinguish tumor-specific and tissue-specific antigen expression on human neuroblastoma cells.
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PMID:Expression by human neuroblastoma cells of an antigen recognized by naturally occurring mouse anti-brain autoantibody. 114 52

A grossly cystic retinoblastoma, presumably a form of the diffuse infiltrating type, mimicked uveitis in an 81/2-year-old boy. A review of 44 cases indicated that grossly (clinically) detectably cysts are rare in this neoplasm, although microcysts are relatively common. Lesions of this nature, especially if presenting with a history of trauma, as in our patient, may lead the ophthalmologist to diagnose uveitis. The diagnosis of retinoblastoma may thus be unduly delayed.
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PMID:Cystic retinoblastoma. 119 Feb 84

Despite considerable advances in the treatment of retinoblastoma tumor growths cannot be arrested in a proportion of cases. The consent fro the removal of both eyes constitutes a burdensome decision on the part of the child's parents, so that it is quite frequently refused. A short movie illustrating the behaviour of a 6-year-old boy, who had undergone bilateral enucleation because of retinoblastoma should aid the parents having to face a similar situation.
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PMID:[Problems concerning the enucleation of both eyes in cases of incurable retinoblastoma (author's transl)]. 122 27

A late diagnosis of retinoblastoma is an unquestionable fact that allows its growth and leads to a deterioration in the outlook. It also gives way to the invasion of the choroidea by the retinal tumor. This event has been related by some authors to orbital recurrences or distant metastases. The evolution of intraocular retinoblastomas, with and without invasion to choroidea, is compared in this work. No significant differences were found in the thirty-three cases studied.
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PMID:[Retinoblastoma. Relation between choroid infiltration and orbital metastasis]. 124 75

Contact B- scan ultrasonography (Bronson-Turner unit) was performed on fourteen patients with retinoblastoma. In ten cases, the patient presented with leukocoria, and ultrasonography was helpful in confirming the clinical diagnosis. In four atypical cases contact B-scan ultrasonography was instrumental in making the diagnosis. The ultrasonographic pattern for retinoblastoma is characteristic but not pathognomic. There is a solid intraocular echo corresponding to the tumor and within it are numerous dense focal echoes which persist at lower sensitivities, suggesting calcification. Calcification was demonstrated ultrasonographically and confirmed histologically in all four of these atypical cases, but routine skull x-rays failed to demonstrate calcium in three of the four children. Contact B- scan ultrasonography is a safe and simple procedure which may provide valuable diagnostic information in children with suspected retinoblastoma.
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PMID:B-scan ultrasonography in the diagnosis of atypical retinoblastomas. 124 38

In examination of six retinoblastoma tumor specimens, bizzare mitochondria were often found. Some are irregular forms with focal expansion and constrictions. Occasionally, a portion of the mitochondria forms rings. Branching mitochondria are also seen. Other striking features of the mitochondria from tumor cells are the alternation of cristae. Dense bodies are also occasionally observed within the mitochondria. Morphological modifications of the mitochondria may be as results of pathological conditions of the tumor cells.
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PMID:Abnormal mitochondria in retinoblastoma. 127 20

Retinoblastoma is a highly malignant intraocular tumor of children that requires accurate diagnosis to prompt treatment. This article reviewed clinical, pathological and follow-up data on 1 147 cases of retinoblastoma registered in Japan from 1975 to 1982. It is obvious that the prognosis of children with retinoblastoma has improved remarkably in recent years. The current advances in the management of the retinoblastoma were discussed.
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PMID:Advances in management of retinoblastoma. 128 78

Retinoblastoma in nude mice as an animal model was developed by injecting cultured human retinoblastoma cell line(Rb) Y79 into the anterior chamber of eyeball. It was treated by direct injection of RGNTF-McAb into the Rb tumor. Ten out of 30 eyeballs with Rb inoculation did not develop tumor (32% inhibition) if Rb cell suspension was mixed with the RGNTF-McAb before injection; whereas in the control, all 40 but 3 eyeballs developed tumor (7%) when Rb cell suspension alone had been injected. This 32% of inhibition of Rb tumor formation by RGNTF-McAb was very significant (T > 2.58, P < 0.01). The results of immunotherapy of 46 eyeballs with Rb tumor developed 10 days after inoculation by RGNTF-McAb for 2 months revealed that the proportion of grade III-IV tumors before and after therapy reduced from 53% to 26% and that of grade I-II tumors increased from 47% to 74%. Feulgen DNA staining of tumor sections after therapy revealed that the average DNA contents in Rb cells decreased significantly (P < 0.01) from 16.2 +/- 2.6 in grade III-IV to 5.3 +/- 1.2 in grade I-II compared to that of the untreated control 18.8 +/- 3.2. Numerous white cells infiltrating the Rb tumor, hyperplasia of fibrous tissues, and no spreading and metastasis of the tumor tissue were observed in the treated eyeballs; whereas Rb tumor was spreading to the optic nerve and superior colliculus in the untreated eyeballs. Therefore, the RGNTF-McAb can not only inhibit the growth of Rb cells but also limit their spreading and metastasis.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:[Immunotherapy of human retinoblastoma with RGNTF-monoclonal antibody using nude mice as model]. 129 Dec 87


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