Junctional nevus: Difference between revisions

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Evaluation: Expanded
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Yes, multifocal and/or in periphery
Yes, multifocal and/or in periphery
|-
|-
|rowspan=4| Cellular<br>''(high<br>mag.)'' || Nuclear pleomorphism<ref name="HusainMein2011">{{cite journal|last1=Husain|first1=Ehab A|last2=Mein|first2=Charles|last3=Pozo|first3=Lucia|last4=Blanes|first4=Alfredo|last5=Diaz-Cano|first5=Salvador J|title=Heterogeneous topographic profiles of kinetic and cell cycle regulator microsatellites in atypical (dysplastic) melanocytic nevi|journal=Modern Pathology|volume=24|issue=4|year=2011|pages=471–486|issn=0893-3952|doi=10.1038/modpathol.2010.143}}</ref> || Slight ||colspan=2| Prominent
| Extended rete pegs || Yes, regular || Yes, varying || Yes, often irregular || Varying, flattened
|-
| Concentric fibrosis || Yes || Yes || Yes || Varies
|-
|-
| Chromatin pattern<ref name="HusainMein2011"/> ||colspan=2| Usually thin || Usually granular
| Lamellar fibrosis || Rarely || Often || Often pronounced || Varying
|-
|-
| Nucleolus<ref name="HusainMein2011"/> ||colspan=2| Usually inconspicuous || Usually prominent
| Lymphocytic infiltrate || Mild, perivascular || Mild or moderate, perivascular || Varying || Varying
|-
|-
| Histological regression<ref name="HusainMein2011"/><ref group="notes">Histological regression is one or more areas within a tumor in which neoplastic cells have disappeared or decreased in number. In this case, this means complete or partial disappearance from areas of the dermis (and occasionally from the epidermis), which have been replaced by fibrosis, accompanied by melanophages, new blood vessels, and a variable degree of inflammation.<br>- {{cite journal|last1=Ribero|first1=Simone|last2=Gualano|first2=Maria Rosaria|last3=Osella-Abate|first3=Simona|last4=Scaioli|first4=Giacomo|last5=Bert|first5=Fabrizio|last6=Sanlorenzo|first6=Martina|last7=Balagna|first7=Elena|last8=Fierro|first8=Maria Teresa|last9=Macripò|first9=Giuseppe|last10=Sapino|first10=Anna|last11=Siliquini|first11=Roberta|last12=Quaglino|first12=Pietro|title=Association of Histologic Regression in Primary Melanoma With Sentinel Lymph Node Status|journal=JAMA Dermatology|volume=151|issue=12|year=2015|pages=1301|issn=2168-6068|doi=10.1001/jamadermatol.2015.2235}}</ref> ||colspan=2| Usually || Usually not
|  
<!--
Most prevalent
Dominant
atypigrad
Easy
Easy-moderate
Moderate-severe
Moderate-severe
cellular
atypia *
Percentage of atypical
melanocytes
<10%
about 10 - 50%
about 50-90%
Usually> 90%
Extended retelists
Yes,
regular
Yes, varying
Yes, often
irregular
Varying,
planarized
Concentric fibrosis Yes Yes Yes Varies
Lamellar fibrosis Rarely Often Often Pronounced Varying
lymphocytic *
Sparingly,
perivascular
Easy-moderate
perivascular
Varying
Varying
reactive
reactive
changes
changes
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Rarely
Rarely
Varying
Varying
Melanocytic atypia
No
Rarely, in superficial
part
Can be detected in
superficial part
Can be detected in
superficial part.
intradermal
component
maturation
Yes
Yes, can be
partial
Yes, can be
partial
Yes, can be
partial; if
No
ripening
recital
invasive
melanoma!
! Further workup !!  !!  !!  Immunohistochemistry
|}




-->
 
|-
|rowspan=4| Cellular<br>''(high<br>mag.)'' || Nuclear pleomorphism<ref name="HusainMein2011">{{cite journal|last1=Husain|first1=Ehab A|last2=Mein|first2=Charles|last3=Pozo|first3=Lucia|last4=Blanes|first4=Alfredo|last5=Diaz-Cano|first5=Salvador J|title=Heterogeneous topographic profiles of kinetic and cell cycle regulator microsatellites in atypical (dysplastic) melanocytic nevi|journal=Modern Pathology|volume=24|issue=4|year=2011|pages=471–486|issn=0893-3952|doi=10.1038/modpathol.2010.143}}</ref> || Slight ||colspan=2| Prominent
|-
| Chromatin pattern<ref name="HusainMein2011"/> ||colspan=2| Usually thin || Usually granular
|-
| Nucleolus<ref name="HusainMein2011"/> ||colspan=2| Usually inconspicuous || Usually prominent
|-
| Histological regression<ref name="HusainMein2011"/><ref group="notes">Histological regression is one or more areas within a tumor in which neoplastic cells have disappeared or decreased in number. In this case, this means complete or partial disappearance from areas of the dermis (and occasionally from the epidermis), which have been replaced by fibrosis, accompanied by melanophages, new blood vessels, and a variable degree of inflammation.<br>- {{cite journal|last1=Ribero|first1=Simone|last2=Gualano|first2=Maria Rosaria|last3=Osella-Abate|first3=Simona|last4=Scaioli|first4=Giacomo|last5=Bert|first5=Fabrizio|last6=Sanlorenzo|first6=Martina|last7=Balagna|first7=Elena|last8=Fierro|first8=Maria Teresa|last9=Macripò|first9=Giuseppe|last10=Sapino|first10=Anna|last11=Siliquini|first11=Roberta|last12=Quaglino|first12=Pietro|title=Association of Histologic Regression in Primary Melanoma With Sentinel Lymph Node Status|journal=JAMA Dermatology|volume=151|issue=12|year=2015|pages=1301|issn=2168-6068|doi=10.1001/jamadermatol.2015.2235}}</ref> ||colspan=2| Usually || Usually not
|-
| Percentage of atypical melanocytes<ref name=KVAST/> || <10% || About 10 - 50% || about 50-90% || Usually> 90%
|-
| Intradermal melanocytic atypia<ref name=KVAST/> || No || Rarely, in superficial part || Can be detected in superficial part || Can be detected in
|-
| Intradermal melanocyte maturation<ref name=KVAST/> || Yes || Yes, can be partial || Yes, can be partial || Yes, can be || Variable
|-
! Further workup !!  !!  !!  Immunohistochemistry<ref name=KVAST/>
|}
|}
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Revision as of 03:50, 24 September 2019

Author: Mikael Häggström [note 1]
Suspected dysplastic nevus (also called dysplastic melanocytic nevus).

Evaluation

Review of clinical information, mainly:[1]

  • Growth
  • Abnormal visual appearance
  • Size >10mm

Microscopy:
Mandatory findings:[1]

  • Shoulder phenomenon, meaning that the extent of the dermal component is larger than the epidermal component.
  • Lentiginous proliferation, meaning an increased amount of melanocytes in the basal area, along rete pegs and sometimes between them.
  • Irregularly distributed nests of melanocytes.
  • Atypia

Classify into either of the following:

Parameter Low-grade dysplasia High-grade dysplasia Suspected melanoma in situ
Mild Moderate Severe
Structural
(Low
mag.)
Delimitation[1] Rarely diffuse Sometimes diffuse Often diffuse
Lentiginous proliferation[notes 1][1] Yes, along with rete pegs Yes, along with and focally between rete pegs Yes, along with and focally between rete pegs Yes partially continuous, multilayered
File:Histopathology of lentigo maligna.jpg
Bridging[1] Rarely Often
Confluent nests[1] Rarely Sometimes Often Often widespread
Pigment distribution[1] Regular Irregular
Suprabasal presence[1] (less than most superficial third of epidermis) No Yes Yes, multifocal
Pagetoid migration including superficial third of epidermis[1] No No Yes, in a maximum of 2 HPF centrally, but not peripherally

Yes, multifocal and/or in periphery

Extended rete pegs Yes, regular Yes, varying Yes, often irregular Varying, flattened
Concentric fibrosis Yes Yes Yes Varies
Lamellar fibrosis Rarely Often Often pronounced Varying
Lymphocytic infiltrate Mild, perivascular Mild or moderate, perivascular Varying Varying

reactive changes regressive changes No No Rarely Varying


Cellular
(high
mag.)
Nuclear pleomorphism[2] Slight Prominent
Chromatin pattern[2] Usually thin Usually granular
Nucleolus[2] Usually inconspicuous Usually prominent
Histological regression[2][notes 2] Usually Usually not
Percentage of atypical melanocytes[1] <10% About 10 - 50% about 50-90% Usually> 90%
Intradermal melanocytic atypia[1] No Rarely, in superficial part Can be detected in superficial part Can be detected in
Intradermal melanocyte maturation[1] Yes Yes, can be partial Yes, can be partial Yes, can be Variable
Further workup Immunohistochemistry[1]

Notes

  1. Lentiginous proliferation is proliferation along the basal layer of the epidermis
  2. Histological regression is one or more areas within a tumor in which neoplastic cells have disappeared or decreased in number. In this case, this means complete or partial disappearance from areas of the dermis (and occasionally from the epidermis), which have been replaced by fibrosis, accompanied by melanophages, new blood vessels, and a variable degree of inflammation.
    - Ribero, Simone; Gualano, Maria Rosaria; Osella-Abate, Simona; Scaioli, Giacomo; Bert, Fabrizio; Sanlorenzo, Martina; Balagna, Elena; Fierro, Maria Teresa; et al. (2015). "Association of Histologic Regression in Primary Melanoma With Sentinel Lymph Node Status ". JAMA Dermatology 151 (12): 1301. doi:10.1001/jamadermatol.2015.2235. ISSN 2168-6068. 
  1. For a full list of contributors, see article history. Creators of images are attributed at the image description pages, seen by clicking on the images. See Patholines:Authorship for details.

Main page

References

  1. 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 Katarzyna Lundmark, Britta Krynitz, Ismini Vassilaki, Lena Mölne, Annika Ternesten Bratel. Histopatologisk bedömning och gradering av dysplastiskt nevus samt gränsdragning mot melanom in situ/melanom (Histopathological assessment and grading of dysplastic nevus and distinction from melanoma in situ/melanoma). KVAST (Swedish Society of Pathology). Retrieved on 2019-09-18.
  2. 2.0 2.1 2.2 2.3 Husain, Ehab A; Mein, Charles; Pozo, Lucia; Blanes, Alfredo; Diaz-Cano, Salvador J (2011). "Heterogeneous topographic profiles of kinetic and cell cycle regulator microsatellites in atypical (dysplastic) melanocytic nevi ". Modern Pathology 24 (4): 471–486. doi:10.1038/modpathol.2010.143. ISSN 0893-3952. 

Image sources