Scholars@Duke
Kenneth Scott Ellington

Kenneth Scott Ellington

Assistant Professor of Pathology
Pathology
kenneth.ellington@duke.edu
Duke Box 3712, Durham, NC 27710
3643 N Roxboro St, Durham, NC 27704-2702

Selected Publications

Rapidly Growing Congenital Groin Mass.

Journal Article Pediatr Dermatol · May 2017 Full text Link to item Cite

Atypical Fibroxanthoma of the Bulbar Conjunctiva.

Journal Article Cornea · December 2015 PURPOSE: To report a rare case of atypical fibroxanthoma (AFX) of the bulbar conjunctiva, and to compare it with previously published cases of conjunctival AFX. METHODS: A 37-year-old woman developed a growth on the bulbar conjunctiva of her left eye that ... Full text Open Access Link to item Cite

Liposarcoma presenting as an intraluminal ureteral mass.

Journal Article Urology · May 2003 An 86-year-old woman with a previous excision of a large retroperitoneal low-grade liposarcoma presented with a 4-month history of persistent left flank discomfort. Workup revealed left hydronephrosis secondary to obstruction, which was caused by a recurre ... Full text Link to item Cite

Adult cellular rhabdomyoma of the heart: a report of 3 cases.

Journal Article Hum Pathol · November 2002 We present 3 adults with cardiac rhabdomyomas, 2 in the atria and 1 in the right ventricle. One atrial tumor was discovered incidentally, and 1 resulted in supraventricular tachycardia. The ventricular lesion caused ventricular tachycardia. Compared with c ... Full text Link to item Cite

MRI of papillary meningiomas in children.

Journal Article Pediatr Radiol · November 1995 We report two cases of papillary meningioma in children. The MRI appearance of this special type of meningioma is described for the first time. Both lesions were dura based and associated with cystic components. We review the literature pertaining to this ... Link to item Cite

Shadow cells in an intracranial dermoid cyst.

Journal Article Arch Pathol Lab Med · April 1995 A case of an intracranial dermoid cyst containing shadow cells is presented. This case expands the group of lesions in which shadow cells, indicative of hair matrical differentiation, have been described. ... Link to item Cite

Walker-Warburg syndrome.

Journal Article AJNR Am J Neuroradiol · 1992 The Walker-Warburg syndrome (WWS) is a rare autosomal recessive disorder characterized by lissencephaly, cerebellar and retinal malformations, and congenital muscular dystrophy. We report a new case of WWS identified with the aid of cranial MR and briefly ... Link to item Cite