Congenital plate-like osteoma cutis of the forehead: an atypical presentation form

Tresserra, L; Tresserra, Francisco; Grases, Pedro; J, Badosa; Tresscrra, Marta

doi:10.1016/s1010-5182(98)80048-6

Cited by 26 publications

(24 citation statements)

References 15 publications

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“…The first was a child with widespread ossification involving the forehead and extraocular muscles. 4 The second was remarkably similar to our two patients and again involved an isolated lesion on the lateral canthus of a 10-month-old girl. 7 The lateral canthus as the site of involvement in the two cases reported here as well as the aforementioned case could be coincidental, yet it raises the possibility of an embryologic explanation that is yet to be determined.…”

Section: Discussionsupporting

confidence: 83%

“…2,4 Congenital platelike cutaneous osteoma is always present within the first year of life, without a predisposing event or abnormality of calcium and phosphorus, but with at least one bony plate. 4 Multiple miliary osteomas of the face usually occur in young women and its relationship to acne vulgaris remains unclear. 3,5 Secondary osteoma cutis is associated with a preexisting lesion and is significantly more common.…”

Section: Discussionmentioning

confidence: 99%

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Congenital osteoma cutis of the lateral canthus

Gupta

Cogen

Metz

2009

Journal of American Association for Pediatric Ophthalmology and

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Section: Discussionsupporting

confidence: 83%

Section: Discussionmentioning

confidence: 99%

Congenital osteoma cutis of the lateral canthus

Gupta

Cogen

Metz

2009

Journal of American Association for Pediatric Ophthalmology and

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“…POH is distinct from other disorders of primary heterotopic ossification, such as platelike osteoma cutis (POC) and fibrodysplasia ossificans progressiva (FOP; OMIM 135100). In POC, cutaneous lesions are present at birth or during the first year of life (19). Patients with POC are character ized by at least one bony plate, plus or minus cutaneous osteomas.…”

Section: Discussionmentioning

confidence: 99%

Progressive osseous heteroplasia, as an isolated entity or overlapping with Albright hereditary osteodystrophy

Lin

Numbenjapon

Germain‐Lee³

et al. 2015

Journal of Pediatric Endocrinology and Metabolism

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“…Osteoma cutis is associated with normal serum levels of calcium and phosphorus throughout life, which suggests that the mutation is on the paternal GNAS allele 41,58,59,[80][81][82] .…”

Section: The Definition Of Pth Resistance Is As Followsmentioning

confidence: 99%

“…Surgical removal of the ectopic ossifications can be performed when the lesions are well delimited. This is rarely the case in patients with POH, but it can be effective in those with osteoma cutis and in superficial lesions associated with PPHP or PHP1A with successful long-term results 58,59,81,241 . In most cases, surgical resection is followed by recurrence or complications 3,83,[242][243][244][245] .…”

Section: Management Of Ectopic Ossificationsmentioning

confidence: 99%

Diagnosis and management of pseudohypoparathyroidism and related disorders: first international consensus statement

Mantovani¹,

Lecumberri²,

Baştepe³

et al. 2018

EJEA

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Pseu do hy popar ath yroi dism (PHP) and related disorders are associated with a spectrum of abnormal physical characteristics as well as neurocognitive and endocrine abnormalities that are caused primarily by molecular defects that impair hormonal signalling via receptors that are coupled, through the α-subunit of the stimulatory G protein (G s α), to activation of adenylyl cyclase (Fig. 1). 6,7,20,48 * Abstract | This Consensus Statement covers recommendations for the diagnosis and management of patients with pseu do hy popar ath yroi dism (PHP) and related disorders, which comprise metabolic disorders characterized by physical findings that variably include short bones, short stature, a stocky build, early-onset obesity and ectopic ossifications, as well as endocrine defects that often include resistance to parathyroid hormone (PTH) and TSH. The presentation and severity of PHP and its related disorders vary between affected individuals with considerable clinical and molecular overlap between the different types. A specific diagnosis is often delayed owing to lack of recognition of the syndrome and associated features. The participants in this Consensus Statement agreed that the diagnosis of PHP should be based on major criteria, including resistance to PTH, ectopic ossifications, brachydactyly and early-onset obesity. The clinical and laboratory diagnosis should be confirmed by a molecular genetic analysis. Patients should be screened at diagnosis and during follow-up for specific features, such as PTH resistance, TSH resistance, growth hormone deficiency , hypogonadism, skeletal deformities, oral health, weight gain, glucose intolerance or type 2 diabetes mellitus, and hypertension, as well as subcutaneous and/or deeper ectopic ossifications and neurocognitive impairment. Overall, a coordinated and multidisciplinary approach from infancy through adulthood, including a transition programme, should help us to improve the care of patients affected by these disorders.

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Congenital plate-like osteoma cutis of the forehead: an atypical presentation form

Cited by 26 publications

References 15 publications

Congenital osteoma cutis of the lateral canthus

Congenital osteoma cutis of the lateral canthus

Progressive osseous heteroplasia, as an isolated entity or overlapping with Albright hereditary osteodystrophy

Diagnosis and management of pseudohypoparathyroidism and related disorders: first international consensus statement

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