2018
DOI: 10.1097/dad.0000000000001118
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Pilomatrixoma: A Comprehensive Review of the Literature

Abstract: Pilomatrixomas are thought to arise from mutation in the Wnt pathway and has been linked to several genetic conditions. It is commonly misdiagnosed preoperatively; however, with better awareness of the lesion, it can be appropriately treated while avoiding unnecessary diagnostic tests. Complete surgical excision with clear margins is almost always curative.

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Cited by 119 publications
(213 citation statements)
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“…Basaloid cells are predominant in the early stages; however, in the later stages, the proportion of shadow cells with accompanying calcification becomes greater [10]. Pilomatricomas are more likely to be resected at an early stage [2] when internal calcification is limited, which may pose some difficulties in terms of the differential diagnosis, as reported previously [9].…”
Section: Discussionmentioning
confidence: 87%
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“…Basaloid cells are predominant in the early stages; however, in the later stages, the proportion of shadow cells with accompanying calcification becomes greater [10]. Pilomatricomas are more likely to be resected at an early stage [2] when internal calcification is limited, which may pose some difficulties in terms of the differential diagnosis, as reported previously [9].…”
Section: Discussionmentioning
confidence: 87%
“…Moreover, there are tumors that occur almost exclusively on the auricle, such as benign and malignant tumors, originating from the ceruminous gland [7]. Pilomatricoma, also known as calcified epithelioma of Malherbe, is unique as its hallmark is internal calcification [2]. In one case series, histopathological examination identified either calcification or ossification in 81% of the tumors [3].…”
Section: Discussionmentioning
confidence: 99%
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