Further Documentation of Spontaneous Regression of Infantile Digital Fibromatosis
: Infantile digital fibromatosis is a rare benign fibromatous tumor characterized by both its location on fingers and toes and its distinctive light microscopic appearance. However, treatment modalities are not yet standardized. Surgical excision had been preferred in the past but has the disadvant...
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Published in: | Pediatric dermatology Vol. 24; no. 3; pp. 280 - 284 |
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Oxford, UK
Blackwell Publishing Ltd
01-05-2007
Blackwell |
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Abstract | : Infantile digital fibromatosis is a rare benign fibromatous tumor characterized by both its location on fingers and toes and its distinctive light microscopic appearance. However, treatment modalities are not yet standardized. Surgical excision had been preferred in the past but has the disadvantage of a high recurrence rate. More recently, isolated instances of spontaneous regression have been reported with a short follow‐up. We report four children with infantile digital fibromatosis, who underwent spontaneous regression after clinical monitoring and long‐term follow‐up. We recommend regular follow‐up in order to allow for intervention in case of functional impact on the affected extremities. |
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AbstractList | Infantile digital fibromatosis is a rare benign fibromatous tumor characterized by both its location on fingers and toes and its distinctive light microscopic appearance. However, treatment modalities are not yet standardized. Surgical excision had been preferred in the past but has the disadvantage of a high recurrence rate. More recently, isolated instances of spontaneous regression have been reported with a short follow-up. We report four children with infantile digital fibromatosis, who underwent spontaneous regression after clinical monitoring and long-term follow-up. We recommend regular follow-up in order to allow for intervention in case of functional impact on the affected extremities. : Infantile digital fibromatosis is a rare benign fibromatous tumor characterized by both its location on fingers and toes and its distinctive light microscopic appearance. However, treatment modalities are not yet standardized. Surgical excision had been preferred in the past but has the disadvantage of a high recurrence rate. More recently, isolated instances of spontaneous regression have been reported with a short follow‐up. We report four children with infantile digital fibromatosis, who underwent spontaneous regression after clinical monitoring and long‐term follow‐up. We recommend regular follow‐up in order to allow for intervention in case of functional impact on the affected extremities. |
Author | Niamba, Pascal Taïeb, Alain Léauté‐Labrèze, Christine Boralevi, Frank Chamaillard, Mélanie Vergnes, Pierre Lepreux, Sébastien |
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Cites_doi | 10.3109/15513819109064791 10.1111/j.1346-8138.1998.tb02448.x 10.1111/j.1365-2133.1989.tb01409.x 10.1002/1096-8628(20000911)94:2<102::AID-AJMG2>3.0.CO;2-X 10.1046/j.1524-4725.2002.02072.x 10.1055/s-2008-1071189 10.1097/01241398-198609000-00017 10.1046/j.1525-1470.2002.02092.x 10.1053/jpsu.2001.27064 |
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Keywords | Human Pseudotumor Pediatrics Dermatology Spontaneous Regression Infant Benign neoplasm Child Fibromatosis |
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References | 2000; 94 2002; 28 2006 2002; 19 1991; 11 2001; 36 1965; 80 1995; 8 1989; 121 1997; 7 1998; 25 1986; 6 e_1_2_4_10_2 e_1_2_4_11_2 e_1_2_4_12_2 e_1_2_4_13_2 e_1_2_4_4_2 Reye RD (e_1_2_4_3_2) 1965; 80 Grazia M (e_1_2_4_2_2) 2006 e_1_2_4_6_2 e_1_2_4_5_2 Hayashi T (e_1_2_4_8_2) 1995; 8 e_1_2_4_7_2 e_1_2_4_9_2 |
References_xml | – volume: 28 start-page: 959 year: 2002 end-page: 961 article-title: Infantile digital fibroma treated with Mohs micrographic surgery publication-title: Dermatol Surg – volume: 25 start-page: 523 year: 1998 end-page: 526 article-title: A case of infantile digital fibromatosis with spontaneous regression publication-title: J Dermatol – volume: 11 start-page: 569 year: 1991 end-page: 588 article-title: Fibroblastic–myofibroblastic tumors in children and adolescents: a clinicopathologic study of 108 examples in 103 patients publication-title: Pediatr Pathol – volume: 36 start-page: 1587 year: 2001 end-page: 1589 article-title: Infantile digital fibromatosis: an unusual localization publication-title: J Pediatr Surg – volume: 7 start-page: 345 year: 1997 end-page: 348 article-title: Infantile digital fibroma—report on eleven cases publication-title: Eur J Pediatr Surg – volume: 19 start-page: 462 year: 2002 end-page: 463 article-title: A case of congenital infantile digital fibromatosis publication-title: Pediatr Dermatol – start-page: 935 year: 2006 end-page: 956 – volume: 6 start-page: 612 year: 1986 end-page: 617 article-title: Recurring digital fibrous tumor of childhood: case report with long‐term follow‐up and review of the literature publication-title: J Pediatr Orthop – volume: 94 start-page: 102 year: 2000 end-page: 112 article-title: Terminal osseous dysplasia and pigmentary defects: clinical characterization of a novel male lethal X‐linked syndrome publication-title: Am J Med Genet – volume: 121 start-page: 129 year: 1989 end-page: 133 article-title: A case of infantile digital fibromatosis showing spontaneous regression publication-title: Br J Dermatol – volume: 80 start-page: 228 year: 1965 end-page: 231 article-title: Recurring digital fibrous tumors of childhood publication-title: Arch Pathol – volume: 8 start-page: 548 year: 1995 end-page: 552 article-title: Infantile digital fibromatosis: a study of the development and regression of cytoplasmic inclusion bodies publication-title: Mod Pathol – ident: e_1_2_4_6_2 doi: 10.3109/15513819109064791 – start-page: 935 volume-title: Textbook of pediatric dermatology year: 2006 ident: e_1_2_4_2_2 contributor: fullname: Grazia M – ident: e_1_2_4_11_2 doi: 10.1111/j.1346-8138.1998.tb02448.x – ident: e_1_2_4_9_2 doi: 10.1111/j.1365-2133.1989.tb01409.x – ident: e_1_2_4_4_2 doi: 10.1002/1096-8628(20000911)94:2<102::AID-AJMG2>3.0.CO;2-X – volume: 8 start-page: 548 year: 1995 ident: e_1_2_4_8_2 article-title: Infantile digital fibromatosis: a study of the development and regression of cytoplasmic inclusion bodies publication-title: Mod Pathol contributor: fullname: Hayashi T – ident: e_1_2_4_12_2 doi: 10.1046/j.1524-4725.2002.02072.x – volume: 80 start-page: 228 year: 1965 ident: e_1_2_4_3_2 article-title: Recurring digital fibrous tumors of childhood publication-title: Arch Pathol contributor: fullname: Reye RD – ident: e_1_2_4_10_2 doi: 10.1055/s-2008-1071189 – ident: e_1_2_4_13_2 doi: 10.1097/01241398-198609000-00017 – ident: e_1_2_4_5_2 doi: 10.1046/j.1525-1470.2002.02092.x – ident: e_1_2_4_7_2 doi: 10.1053/jpsu.2001.27064 |
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Snippet | : Infantile digital fibromatosis is a rare benign fibromatous tumor characterized by both its location on fingers and toes and its distinctive light... Infantile digital fibromatosis is a rare benign fibromatous tumor characterized by both its location on fingers and toes and its distinctive light microscopic... |
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SubjectTerms | Biological and medical sciences Child Dermatology Female Fibroma - pathology Fibroma - surgery Fingers General aspects Humans Infant Male Medical sciences Recurrence Remission, Spontaneous Skin Neoplasms - pathology Skin Neoplasms - surgery Toes |
Title | Further Documentation of Spontaneous Regression of Infantile Digital Fibromatosis |
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