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At least 19 recordsLinked to original sources

Phakomatous choristoma of the eyelid. Immunohistochemical and electron microscopic observations.

BACKGROUND: A 13-month-old Hispanic boy underwent excision of a congenital inferonasal orbital mass arising from the right lower lid. Results of histopathologic examination of the tumor showed a phakomatous choristoma of the eyelid. An immunohistochemical and electron microscopic study of this rare, benign, congenital tumor of lenticular anlage was performed. METHODS: Immunohistochemistry was performed on 4-microns thick sections from paraffin-embedded tissue. Electron microscopy was performed on thin sections stained with uranyl acetate and lead citrate. FINDINGS: The cuboidal epithelial cells that comprise this choristoma showed strongly positive cytoplasmic staining with S-100 protein and vimentin and focally positive staining with a keratin cocktail (AE1/AE3). Electron microscopy showed the presence of numerous 10-nm whorled cytoplasmic microfilaments within degenerating epithelial cells. CONCLUSION: The immunoreactivity of this tumor to keratin and vimentin are newly described in this detailed clinicopathologic report and, together with its S-100 positivity, support the proposal that this tumor is of lenticular anlage. The authors hypothesize that the intracytoplasmic 10-nm intermediate filaments observed with electron microscopic examination within the epithelial cells that comprise this choristoma represent vimentin as detected by immunohistochemistry.

Choristoma

Osseous choristoma of the choroid.

A case is presented in which the diagnosis was made clinically of an osseous lesion of the choroid in an otherwise normal eye. The clinical diagnosis of an osseous choristoma was confirmed by the use of ultrasonography, orbital roentgenograms, and computerized axial tomography. Enlargement of the lesion was documented photographically during a four-month period. The causes of intraocular ossification are discussed, and the typical clinical features of osseous choristoma of the choroid are suggested.

Adolescent

Osseous choristoma of the choroid simulating a choroidal melanoma. Association with a positive 32P test.

We report the clinical and histopathologic features of an osseous choristoma of the choroid that appeared in a 26-year-old woman. Her diagnostic evaluation included a radioactive phosphorus (32P) uptake test, which was 270% positive and led us to believe that the lesion was an atypical malignant melanoma. The extent of true ossification within this tumor, seen microscopically, explains the false-positive uptake of radioactive phosphorus by this benign tumor; it is well known that bone avidly accumulates radioactive phosphorus. We recommend that all "atypical choroidal melanomas" be studied for the presence of bone, with bone-free roentgenograms, ultrasonography, and possibly, computerized tomographic scans before 32P testing or enucleation. This, to our knowledge, is the second histopathologically proved case of an osseous choristoma of the choroid to be reported in the literature.

Adult

Phakomatous choristoma of eyelid: electron microscopical confirmation of lenticular derivation.

This article presents the sixth recorded example of phakomatous choristoma of the eyelid. The tumor occurred in a 4-month-old boy and was located in the lower lid near the inner canthus. The findings from light microscopy included epithelial, tubular structures with associated patches of thick, irregular basement membrane. The results of electron microscopy (ie, epithelial cells with a scarcity of organelles, homogeneous type of basement membrane, cytoplasmic microfilaments, segments of fascia occludens, and degenerated cells with peculiar interdigitations of their plasmalemmas) are all consistent with lenticular derivation, as originally proposed by Zimmerman.

Basement Membrane

Bilateral choristomas of the external auditory canals.

To our knowledge, we report the first case of external auditory canal choristomas in the American literature. The pathologic condition of each side was serous salivary tissue, and at surgery, there was no connection with the parotid gland.

Child

Lingual osseous choristoma. Report of two cases.

The lingual osseous choristoma is a rare benign lesion of the tongue, and it is difficult to make a correct preoperative diagnosis of these lesions. Two cases are presented in this article.

Adolescent

Sebaceous choristoma of the thyroglossal duct.

The presence of sebaceous glands within the oral mucosa is not uncommon. Such Fordyce granules are frequently seen on the buccal mucosa and lips, as well as in the retromolar area, gingiva, and palate. Whereas sebaceous elements are rarely encountered on the tongue, three cases of ectopic sebaceous glands have been reported in association with apparently patent thyroglossal ducts. An interesting case of a previously unreported sebaceous choristoma of the thyroglossal duct is described.

Choristoma

Salivary gland choristoma of the middle ear.

A case is described in which a middle-ear salivary gland choristoma was found in association with dehiscence of the horizontal part of the facial nerve and abnormality of the stapes and incus. It is suggested that these features may constitute an abnormal development syndrome.

Adult

Epipalpebral conjunctival osseous choristoma.

Two cases of osseous choristoma are described. One of the tumours was found in the conjunctiva of the right lower lid, an apparently unique location. The other more typical epibulbar tumour was found in the superior temporal quadrant of the episclera between the lateral and superior rectus muscles. In both instances the tumour was suspected of being a dermoid.

Adolescent

Phakomatous choristoma of lower eyelid. A lenticular anlage tumour.

A female infant was found to have a congenital, firm, pea-sized tumour nasally in the lower left eyelid. A dermoid cyst was suspected, but microscopy showed structures simulating a lens. The tumour has been considered to have an origin in surface ectoderm induced to dip down into the mesoderm of the lid, there forming lenticular anlage structures. This so-called phakomatous choristoma has only been reported five times previously, all cases outside Europe.

Choristoma

Neonatal cystic choristoma in submandibular salivary gland simulating cystic hygroma.

A congenital cystic malformation occurred in the submandibular salivary gland of a neonate. The embryogenesis and differential diagnosis are discussed. Since it seems to be a product of endodermal heterotopic differentiation or entrapment of foregut epithelial rests in the submandibular gland, it is classified as a cystic choristoma.

Choristoma

Salivary gland choristoma of the middle ear.

We discuss the eighth reported case of a benign salivary gland tumor in the middle ear. The lesion was a smooth lobulated mass and was found to be intimately associated with the tympanic portion of the facial nerve. Recommended treatment is biopsy without attempting removal. This concept of management is supported by a report of a similar case with a 15-year follow-up.

Child

A case of salivary gland choristoma of the middle ear.

The authors present a case of tympanic cavity salivary gland adenochoristoma in association with an abnormal course of the facial nerve, absence of the oval and round windows, absence of the stapes, hypoplasia of the long process of the incus, and the existence of a subtympanic bony lamina.

Choristoma