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Journal of the American Academy of... May 1991Postacne osteoma cutis is a rare complication of acne vulgaris. If it occurs during a course of tetracycline or minocycline therapy, pigmented osteomas can occur as a... (Review)
Review
Postacne osteoma cutis is a rare complication of acne vulgaris. If it occurs during a course of tetracycline or minocycline therapy, pigmented osteomas can occur as a result of tetracycline or minocycline bone complexes. We report a case of pigmented postacne osteoma cutis that developed after extensive acne surgery and a 2- to 3-month course of minocycline. Previously reported cases have been treated surgically, but our patient responded to 0.05% tretinoin cream, with transepidermal elimination of some osteomas.
Topics: Acne Vulgaris; Adult; Facial Dermatoses; Facial Neoplasms; Female; Humans; Minocycline; Osteoma; Pigmentation Disorders; Skin Neoplasms
PubMed: 1828815
DOI: 10.1016/0190-9622(91)70131-k -
Journal of Cutaneous Pathology Apr 2023
Topics: Humans; Pseudohypoparathyroidism; Bone Diseases, Metabolic; Skin Diseases, Genetic; Ossification, Heterotopic
PubMed: 36691934
DOI: 10.1111/cup.14397 -
Archives of Dermatology and Syphilology Aug 1948
Topics: Bone Diseases, Metabolic; Humans; Neoplasms; Ossification, Heterotopic; Osteoma; Skin; Skin Diseases, Genetic; Skin Neoplasms
PubMed: 18110543
DOI: 10.1001/archderm.1948.01520210078011 -
Proceedings of the Royal Society of... Feb 1965
Topics: Bone Diseases, Metabolic; Calcinosis; Child; Foot Diseases; Hand Deformities; Humans; Hypoparathyroidism; Ossification, Heterotopic; Osteoma; Pathology; Pseudopseudohypoparathyroidism; Radiography; Skin Diseases; Skin Diseases, Genetic; Skin Neoplasms
PubMed: 14262017
DOI: No ID Found -
BMJ Case Reports May 2014Osteoma cutis encompasses a group of cutaneous ossifying disorders, more commonly secondary to trauma, inflammation or neoplasms. Fourteen per cent, however, are...
Osteoma cutis encompasses a group of cutaneous ossifying disorders, more commonly secondary to trauma, inflammation or neoplasms. Fourteen per cent, however, are primary, and these may be syndromatic (associated to Albright's hereditary osteodystrophy) or occur in isolation. We report a case of a 10-year-old girl who presented with a stone-hard plate on the scalp, with no relevant personal or family history, nor changes in calcium-phosphate metabolism, parathyroid hormone or thyroid function. Skin biopsy confirmed osteoma cutis. Plate-like osteoma cutis is rare, and believed to be a non-progressive form of heterotopic ossification, included in the spectrum of progressive osseus heteroplasia and Albright hereditary osteodystrophy, due to GNAS gene mutations. This recently clarified association should remind us of the possible unfavourable evolution of a seemingly innocent clinical picture, emphasising the need for appropriate evaluation, management and follow-up.
Topics: Bone Diseases, Metabolic; Child; Female; Humans; Ossification, Heterotopic; Scalp Dermatoses; Skin Diseases, Genetic
PubMed: 24798356
DOI: 10.1136/bcr-2013-202901 -
Journal of Paediatrics and Child Health Jul 2022
Topics: Bone Diseases, Metabolic; Humans; Ossification, Heterotopic; Skin Diseases, Genetic
PubMed: 34706128
DOI: 10.1111/jpc.15814 -
The British Journal of Dermatology Nov 1971
Topics: Adolescent; Calcium; Dwarfism; Epilepsy; Female; Humans; Hypocalcemia; Infant; Infant, Newborn; Knee; Male; Ossification, Heterotopic; Phosphorus; Pseudohypoparathyroidism; Radiography
PubMed: 5002319
DOI: 10.1111/j.1365-2133.1971.tb14056.x -
A.M.A. Archives of Dermatology and... May 1954
Topics: Bone Diseases, Metabolic; Humans; Ossification, Heterotopic; Skin Diseases; Skin Diseases, Genetic
PubMed: 13147570
DOI: 10.1001/archderm.1954.01540170083012 -
Plastic and Reconstructive Surgery Mar 2000
Topics: Aged; Hand; Humans; Male; Ossification, Heterotopic; Skin Diseases
PubMed: 10724263
DOI: 10.1097/00006534-200003000-00027 -
Journal of the American Academy of... Feb 1987Platelike osteoma cutis is a rare lesion that is most often congenital. An 85-year-old man developed a plate, or sheet, of subcutaneous bone in an area previously...
Platelike osteoma cutis is a rare lesion that is most often congenital. An 85-year-old man developed a plate, or sheet, of subcutaneous bone in an area previously affected by morphea. The sheet of bone was visualized with a variety of imaging technics, including xerography, computed tomography, and radionuclide bone scans.
Topics: Aged; Aged, 80 and over; Humans; Male; Ossification, Heterotopic; Scleroderma, Localized; Skin; Skin Diseases
PubMed: 3102570
DOI: 10.1016/s0190-9622(87)80005-1