Congenital apocrine hamartoma: an unusual clinical variant of organoid nevus with apocrine differentiation
Congenital apocrine hamartomas are rare tumors of the skin composed of mature apocrine glands in the papillary and reticular dermis. Several cases have been reported in the literature but few were of uniform clinical appearance. The term apocrine nevus has been used interchangeably with apocrine ham...
Saved in:
Published in | Pediatric dermatology Vol. 12; no. 3; p. 248 |
---|---|
Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
01.09.1995
|
Subjects | |
Online Access | Get more information |
Cover
Loading…
Abstract | Congenital apocrine hamartomas are rare tumors of the skin composed of mature apocrine glands in the papillary and reticular dermis. Several cases have been reported in the literature but few were of uniform clinical appearance. The term apocrine nevus has been used interchangeably with apocrine hamartoma in the literature, however, based on their distinctive morphologies we believe they are different entities. We describe a 7-year-old girl with a congenital apocrine hamartoma of the left cheek. A stained biopsy specimen from the lesion revealed large mature apocrine glands with decapitation secretion in the dermis. The presence of periodic acid-Schiff-positive, diastase-resistant granular material in the apical cytoplasm of some secretory cells helped differentiate these as apocrine glands. We think this lesion may represent a form of organoid nevus with pure apocrine differentiation. |
---|---|
AbstractList | Congenital apocrine hamartomas are rare tumors of the skin composed of mature apocrine glands in the papillary and reticular dermis. Several cases have been reported in the literature but few were of uniform clinical appearance. The term apocrine nevus has been used interchangeably with apocrine hamartoma in the literature, however, based on their distinctive morphologies we believe they are different entities. We describe a 7-year-old girl with a congenital apocrine hamartoma of the left cheek. A stained biopsy specimen from the lesion revealed large mature apocrine glands with decapitation secretion in the dermis. The presence of periodic acid-Schiff-positive, diastase-resistant granular material in the apical cytoplasm of some secretory cells helped differentiate these as apocrine glands. We think this lesion may represent a form of organoid nevus with pure apocrine differentiation. |
Author | Herrmann, J J Eramo, L R |
Author_xml | – sequence: 1 givenname: J J surname: Herrmann fullname: Herrmann, J J organization: Department of Pediatrics, Children's Memorial Hospital, Northwestern University Medical School, Chicago, Illinois 60614, USA – sequence: 2 givenname: L R surname: Eramo fullname: Eramo, L R |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/7501558$$D View this record in MEDLINE/PubMed |
BookMark | eNpFj09LAzEQxXOo1Fr9CELwvnWS3Wyy3qT4Dwpe9Fxms5M2pU3KbrbqtzdgwXeZ92aYB78rNgkxEGN3AhYi6363EEqqQlQ6L5pGLVILIHL4nrAZ6LIuDFT1Jbsahh0AmLoWUzbVCoRSZsZ2yxg2FHzCPcdjtL0PxLd4wD7FAz5wDHwM4zDms9374G02J-w9hsSj47HfYIi-44FO48C_fNr-13TeOeopJI_Jx3DNLhzuB7o5zzn7fH76WL4Wq_eXt-XjqrBlY0zRNth2hloUnVYNOFWScNAJYUBrSVZXorbadUI32lZUEWopCSRQafM_yjm7_es9ju2BuvWx9xnnZ31mlr9VCV3C |
CitedBy_id | crossref_primary_10_1097_00000372_199910000_00011 crossref_primary_10_1111_j_1525_1470_2007_00431_x crossref_primary_10_1097_DAD_0b013e31823adf0e |
ContentType | Journal Article |
DBID | CGR CUY CVF ECM EIF NPM |
DOI | 10.1111/j.1525-1470.1995.tb00170.x |
DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) |
DatabaseTitleList | MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | no_fulltext_linktorsrc |
Discipline | Medicine |
ExternalDocumentID | 7501558 |
Genre | Journal Article Case Reports |
GroupedDBID | --- .3N .GA .GJ .Y3 05W 0R~ 10A 123 1OB 1OC 29O 31~ 33P 36B 3SF 4.4 50Y 50Z 51W 51X 52M 52N 52O 52P 52R 52S 52T 52U 52V 52W 52X 53G 5HH 5LA 5RE 5VS 66C 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A01 A03 AAESR AAEVG AAHHS AAKAS AANLZ AAONW AASGY AAXRX AAZKR ABCQN ABCUV ABEML ABJNI ABPPZ ABPVW ABQWH ABXGK ACAHQ ACBWZ ACCFJ ACCZN ACGFS ACGOF ACMXC ACPOU ACPRK ACSCC ACXBN ACXQS ADBBV ADBTR ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZCM ADZMN AEEZP AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFEBI AFFNX AFFPM AFGKR AFPWT AFZJQ AHBTC AHEFC AIACR AITYG AIURR AIWBW AJBDE ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR AMYDB ASPBG ATUGU AVWKF AZBYB AZFZN AZVAB BAFTC BDRZF BFHJK BHBCM BMXJE BROTX BRXPI BY8 C45 CAG CGR COF CS3 CUY CVF CYRXZ D-6 D-7 D-E D-F DCZOG DPXWK DR2 DRFUL DRMAN DRSTM DU5 EBS ECM EIF EJD EMOBN ESX EX3 F00 F01 F04 F5P FEDTE FUBAC FZ0 G-S G.N GODZA H.X HF~ HGLYW HVGLF HZI HZ~ IHE IX1 J0M K48 KBYEO L7B LATKE LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES MEWTI MK4 MRFUL MRMAN MRSTM MSFUL MSMAN MSSTM MXFUL MXMAN MXSTM N04 N05 N9A NF~ NPM O66 O9- OIG OVD P2P P2W P2X P2Z P4B P4D PALCI Q.N Q11 QB0 R.K RIWAO RJQFR ROL RX1 SAMSI SUPJJ TEORI UB1 W8V W99 WBKPD WH7 WHWMO WIH WIJ WIK WOHZO WOW WQJ WRC WUP WVDHM WXI WXSBR XG1 YFH ZGI ZXP ZZTAW ~IA ~WT |
ID | FETCH-LOGICAL-c3988-b9abd8eba1d7590f53e1f0d1180772ec7416c7fd1797c4e4ea722e020e3c988a2 |
ISSN | 0736-8046 |
IngestDate | Sat Sep 28 08:39:33 EDT 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 3 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c3988-b9abd8eba1d7590f53e1f0d1180772ec7416c7fd1797c4e4ea722e020e3c988a2 |
PMID | 7501558 |
ParticipantIDs | pubmed_primary_7501558 |
PublicationCentury | 1900 |
PublicationDate | September 1995 |
PublicationDateYYYYMMDD | 1995-09-01 |
PublicationDate_xml | – month: 09 year: 1995 text: September 1995 |
PublicationDecade | 1990 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | Pediatric dermatology |
PublicationTitleAlternate | Pediatr Dermatol |
PublicationYear | 1995 |
SSID | ssj0008661 |
Score | 1.5021844 |
Snippet | Congenital apocrine hamartomas are rare tumors of the skin composed of mature apocrine glands in the papillary and reticular dermis. Several cases have been... |
SourceID | pubmed |
SourceType | Index Database |
StartPage | 248 |
SubjectTerms | Child Facial Neoplasms - congenital Facial Neoplasms - pathology Female Hamartoma - pathology Humans Nevus - congenital Nevus - pathology Sweat Gland Diseases - congenital Sweat Gland Diseases - pathology Sweat Gland Neoplasms - congenital Sweat Gland Neoplasms - pathology |
Title | Congenital apocrine hamartoma: an unusual clinical variant of organoid nevus with apocrine differentiation |
URI | https://www.ncbi.nlm.nih.gov/pubmed/7501558 |
Volume | 12 |
hasFullText | |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1La8JAEF5qS4uX0pf0zR56CynmsSbprYhFSvWk4E32SVswEatS-us7u9nEVCp9XELMmsXsfDvOTOabQegGnCrCW0q6XLurIWsql4VcuUooHia0Kal5e97rt7rD8HFERmvskjm75R_f8kr-I1W4BnLVLNk_SLacFC7AOcgXjiBhOP5Kxu1MM6N02w-HTjOuiXzOM53AN7OJ6bkDm3eRLt40RaSkQC7BO6Z5AoBp6ZS9CCeVy0XBcysmKlqnzCvCs1Zs2d_DEVqxz7-E5rtypokIOedj9dapM6MTE5Z9sjmKwnLvSJlLVWikyFQvtjHDQn36FZgEVV2Yl9DcrKOJT1wvjAxjkpgQtQcf3qs3wVJNJ0Z6YNmA6RP_OLhWPduO1FAtirUC7Otgjv2jjlumnG75VLYmrU302vDr6mjXzrnmiBiDZHCA9q0nge9zWByiLZkeob2ezZU4Rq8rdOBCqLhExx2mKbbYwAU2sMUGzhQusIENNrDGxmqaNWycoOFDZ9DuurazhsuDBDYRSygTsWTUExFJmooE0lNNocsBgrcluTbTeaQEaOuIhzKUNPJ9CZ6FDDjcT_0G2k6zVJ4inBAGLiv3Y85oGAcS9H_iEQZmI49imogz1MhXaTzNy6eM7fKdbxq4QPUV-C7RjoLdKq_A9JuzayPAT3xTWOo |
link.rule.ids | 786 |
linkProvider | National Library of Medicine |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Congenital+apocrine+hamartoma%3A+an+unusual+clinical+variant+of+organoid+nevus+with+apocrine+differentiation&rft.jtitle=Pediatric+dermatology&rft.au=Herrmann%2C+J+J&rft.au=Eramo%2C+L+R&rft.date=1995-09-01&rft.issn=0736-8046&rft.volume=12&rft.issue=3&rft.spage=248&rft_id=info:doi/10.1111%2Fj.1525-1470.1995.tb00170.x&rft_id=info%3Apmid%2F7501558&rft_id=info%3Apmid%2F7501558&rft.externalDocID=7501558 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0736-8046&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0736-8046&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0736-8046&client=summon |