2000
DOI: 10.1159/000018324
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Three Cases of Type 2 Segmental Manifestation of Multiple Glomus Tumors: Association with Linear Multiple Trichilemmal Cysts in a Patient

Abstract: We report 3 cases of congenital multiple glomus tumors seen during the last 5 years. One of them showed autosomal dominant inheritance with male-to-male transmission. The remaining patients had no family history of similar lesions. The clinical and histopathological aspects of our patients support the recently described type 2 segmental manifestation of multiple glomus tumors. One of the cases showed associated multiple and giant trichilemmal cysts with a linear distribution in the scalp.

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Cited by 25 publications
(19 citation statements)
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“…These findings indicate that the cysts of the present case probably originated from the nonadnexal epidermis. A similar localized distribution of multiple trichilemmal cysts was reported in a case of multiple glomus tumors [17]. The development on the dominant hand suggests that invagination of epidermal cells caused by traumatic injuries induced these palmar epidermoid cysts.…”
Section: Discussionsupporting
confidence: 70%
“…These findings indicate that the cysts of the present case probably originated from the nonadnexal epidermis. A similar localized distribution of multiple trichilemmal cysts was reported in a case of multiple glomus tumors [17]. The development on the dominant hand suggests that invagination of epidermal cells caused by traumatic injuries induced these palmar epidermoid cysts.…”
Section: Discussionsupporting
confidence: 70%
“…A positive family history, not found in our observation, is present in 60% of cases [1]. CMGTs are extremely rare, and less than 20 cases have been well documented [5, 6, 7, 8, 9, 10, 11, 12]. Our case is an uncommon example of congenital glomangiomas which, moreover, occurred sporadically.…”
Section: Discussionsupporting
confidence: 47%
“…Seven case reports of CMGT with a type 2 segmental involvement have been so far recorded in the world literature [6, 8, 10, 11, 12]. In the majority of cases, congenital lesions showed a unilateral distribution whereas tumors developed later in time were disseminated smaller nodules based on the phenotype (table 1).…”
Section: Discussionmentioning
confidence: 99%
“…As a segmental distribution of cutaneous lesions in other diseases, 3 cases with type 2 segmental manifestation of multiple glomus tumors have recently been presented by Florez et al [13], and also 1 each with type 1 or 2 segmental Darier disease by Itin et al [14]. These disorders may easily be differentiated histologically from eccrine spiradenomas.…”
Section: Discussionmentioning
confidence: 99%