Melanoma classification: Difference between revisions

Jump to navigation Jump to search
(Mahshid)
No edit summary
 
Line 3: Line 3:
{{CMG}} {{AE}} {{YD}}; {{SSK}}
{{CMG}} {{AE}} {{YD}}; {{SSK}}
==Overview==
==Overview==
Melanoma may be classified into either cutaneous or non-cutaneous melanomas. The most common 4 subtypes of cutaneous melanoma include superficial spreading melanoma, nodular melanoma, acral lentiginous melanoma, and lentigo maligna melanoma. Less common subtypes of melanoma include desmoplastic/spindle cell melanoma, nevoid melanoma, spitzoid melanocytic melanoma, angiotropic melanoma, blue nevus-like melanoma, and composite melanoma.
[[Melanoma]] may be classified into either [[Skin|cutaneous]] or [[Skin|non-cutaneous]] [[Melanoma|melanomas]]. The most common 4 sub-types of [[Skin|cutaneous]] [[melanoma]] include [[Superficial (human anatomy)|superficial]] spreading [[melanoma]], [[Nodule (medicine)|nodular]] [[melanoma]], [[acral lentiginous melanoma]], and [[lentigo maligna melanoma]]. Less common sub-types of [[melanoma]] include [[Desmoplasia|desmoplastic]]/[[spindle cell]] [[melanoma]], [[nevoid melanoma]], [[Spitzoid melanoma|spitzoid melanocytic melanoma]], [[angiotropic melanoma]], [[blue nevus]]-like [[melanoma]], and [[composite melanoma]].


==Classification of Melanoma==
==Classification of Melanoma==
Shown below is a table that demonstrates that various subclasses of melanoma:<ref name=book1>{{cite book|last=Schanderdorf D, Kochs C, Livingstone E |date=2013 |title=Handbook of Cutaneous Melanoma: A Guide to Diagnosis and Treatment |publisher=Springer }}</ref><ref name=book2>{{cite book|last=Mooi W, Krausz T|date=2007 |title=Pathology of Melanocytic Disorders 2nd Ed. |publisher=CRC Press}}</ref>
Shown below is a table that demonstrates the various sub-classes of [[melanoma]]:<ref name="book1">{{cite book|last=Schanderdorf D, Kochs C, Livingstone E |date=2013 |title=Handbook of Cutaneous Melanoma: A Guide to Diagnosis and Treatment |publisher=Springer }}</ref><ref name="book2">{{cite book|last=Mooi W, Krausz T|date=2007 |title=Pathology of Melanocytic Disorders 2nd Ed. |publisher=CRC Press}}</ref>
{| {{table}}
{| {{table}} cellpadding="4" cellspacing="0" style="border:#c9c9c9 1px solid; margin: 1em 1em 1em 0; border-collapse: collapse;"
| align="center" style="background: #4479BA;" | {{fontcolor|#FFF|'''Subtype'''}}
| align="center" style="background: #4479BA;" | {{fontcolor|#FFF|'''Subtype'''}}
| align="center" style="background: #4479BA;" | {{fontcolor|#FFF|'''Frequency'''}}
| align="center" style="background: #4479BA;" | {{fontcolor|#FFF|'''Frequency'''}}
| align="center" style="background: #4479BA;" | {{fontcolor|#FFF|'''Clinical Features'''}}
| align="center" style="background: #4479BA;" | {{fontcolor|#FFF|'''Clinical Features'''}}
|-
|-
|colspan=3|'''''Common Subtypes'''''
| colspan="3" |'''''Common Subtypes'''''
|-
|-
|Superficial spreading melanoma||70%||
|[[Superficial (human anatomy)|Superficial]] spreading [[melanoma]]||70%||
*Most common subtype
*Most common sub-type
*Usually affects sun exposed sites among both men and women aged 50-70 years
*Usually affects sun exposed sites among both men and women aged 50-70 years
*Characterized by ''presence'' of abundant junctional intraepidermal spread of malignant melanocytes
*Characterized by the ''presence'' of abundant junctional [[Epidermis (skin)|intra-epidermal]] spread of [[malignant]] [[Melanocyte|melanocytes]]
|-
|-
|Nodular melanoma||15-25%||
|[[Nodular melanoma]]||15-25%||
*Second most common subtype
*Second most common subtype
*Usually affects sun exposed sites among both men and women aged 50-70 years
*Usually affects sun exposed sites among both men and women aged 50-70 years
*Characterized by ''absence'' of junctional intraepidermal spread of malignant melanocytes
*Characterized by the ''absence'' of junctional [[Epidermis (skin)|intra-epidermal]] spread of [[malignant]] [[Melanocyte|melanocytes]]
|-
|-
|Acral lentiginous melanoma||5%||
|[[Acral lentiginous melanoma]]||5%||
*Not associated with chronic ultraviolet exposure
*Not associated with [[Chronic (medical)|chronic]] [[ultraviolet]] exposure
*Affects the extremities among inidividuals of all races
*Affects the [[Limb (anatomy)|extremities]] of individuals of all [[Race|races]]
*Common among elderly Caucasian and non-Causasian individuals
*Common among the elderly Caucasian and non-Caucasian individuals
|-
|-
|Lentigo maligna melanoma||1-5%||
|[[Lentigo maligna melanoma]]||1-5%||
*Preceded by lentigo maligna
*Preceded by [[lentigo maligna]]
*Common among elderly Caucasian patients
*Common among the elderly Caucasian [[Patient|patients]]
*Usually appears as a flat, non-palpable lesion that affects sun exposed sites, especially the head and neck (extremities are less common)
*Usually appears as a flat, non-palpable [[lesion]] that affects sun exposed sites, especially the [[head]] and [[neck]] ([[Lesion|lesions]] on [[Limb (anatomy)|extremities]] are less common)
|-
|-
| Non-cutaneous melanoma||5%||
| [[Skin|Non-cutaneous]] [[melanoma]]||5%||
*Melanoma that does not affect the skin
*[[Melanoma]] that does not affect the [[skin]]
*Usually affects the eye (ocular melanoma) or the mucus membranes (mucosal melanoma)
*Usually affects the [[eye]] ([[ocular]] [[melanoma]]) or the [[Mucous membrane|mucus membranes]] ([[Mucous membrane|mucosal]] [[melanoma]])
|-
|-
| colspan=3| '''''Less Common Subtypes'''''
| colspan="3" | '''''Less Common Subtypes'''''
|-
|-
| Desmoplastic/Spindle cell melanoma||Rare||
| [[Desmoplasia|Desmoplastic]]/[[Spindle cell]] [[melanoma]]||Rare||
*Lesion typically amelanotic and has a morphology similar to a scar tissue
*[[Lesion]] typically amelanotic and has a [[morphology]] similar to a [[scar tissue]]
*Appears indolent but is highly infiltrative  
*Appears indolent but is highly [[Infiltration (medical)|infiltrative]]
*Characterized by local recurrence and perineural spread
*Characterized by local recurrence and [[Perineurium|perineural]] spread
*Usually affects males aged 60-70 years in sun exposed sites
*Usually affects males aged 60-70 years in sun exposed sites
*May be de novo or associated with a pre-existing melanoma
*May be [[de novo]] or can be associated with a pre-existing [[melanoma]]
*Has several subtypes:
*Has several subtypes:
::*Pure: paucicellular
::*Pure: paucicellular
::*Desmoplastic-neurotropic melanoma: characterized by neurotropism
::*[[Desmoplasia|Desmoplastic]]-neurotropic [[melanoma]]: characterized by neurotropism
::*Pure neurotropic melanoma: no desmoplasia with spindle cell melanoma of neurotropic phenotype
::*Pure neurotropic [[melanoma]]: no [[desmoplasia]] with [[spindle cell]] [[melanoma]] of neurotropic [[phenotype]]
::*Mixed/Combined: epithelial and spindle cells
::*Mixed/Combined: [[Epithelium|epithelial]] and [[spindle cells]]
|-
|-
| Nevoid melanoma||Rare||
| [[Nevoid melanoma]]||Rare||
*Lesion has features of both melanoma and melanocytic nevus on histopathological analysis
*[[Lesion]] has features of both [[melanoma]] and [[melanocytic nevus]] on [[Histopathology|histopathological]] [[analysis]]
*Clinical features resemble those of typical melanoma
*Clinical features resemble those of a typical [[melanoma]]
|-
|-
| Spitzoid melanocytic neoplasm||Rare||
| [[Spitzoid melanoma|Spitzoid melanocytic neoplasm]]||Rare||
*Lesion has features of both melanoma and Spitz (epithelioid) tumor
*[[Lesion]] has features of both [[melanoma]] and Spitz ([[epithelioid]]) [[tumor]]
*Typically affects sun exposed sites among children and young adults, but adults with Spitz tumors are more often diagnosed with Spitzoid melanoma
*Typically affects sun exposed sites among children and young adults, but adults with Spitz [[Tumor|tumors]] are more often [[Diagnosis|diagnosed]] with [[Spitzoid melanoma]]
*Compared to benign Spitz tumors, Spitzoid melanomas are usually large (>5 mm)
*Compared to [[benign]] Spitz [[Tumor|tumors]], [[Spitzoid melanoma|Spitzoid melanomas]] are usually large (>5 mm)
|-
|-
| Angiotropic melanoma||Rare||
| [[Angiotropic melanoma]]||Rare||
*Lesion characterized by angiotropism, whereby melanoma grows in proximity (within 1-2 mm) to blood and/or lymphatic tissue but no tumor within the vascular lamina itself
*[[Lesion]] characterized by angiotropism, whereby the [[melanoma]] grows in proximity (within 1-2 mm) to [[blood]] and/or [[Lymphatic system|lymphatic tissue]] but no [[tumor]] within the [[vascular]] [[lamina]] itself
*The tumor may originally be another subtype of melanoma
*The [[tumor]] may originally be another sub-type of [[melanoma]]
*Clinical features similar to typical melanoma
*Clinical features similar to typical [[melanoma]]
|-
|-
| Blue nevus-like melanoma||Rare||
| [[Blue nevus]]-like [[melanoma]]||Rare||
*Melanoma that develops from a pre-existing blue nevus
*[[Melanoma]] that develops from a pre-existing [[blue nevus]]
*One of the rarest forms of melanoma
*One of the rarest forms of [[melanoma]]
*Appears as a blue nevus that has recently been rapidly expanding with irregular contours
*Appears as a [[blue nevus]] that has recently been rapidly expanding with irregular contours
*Typically affects middle-aged men
*Typically affects middle-aged men
|-
|-
| Composite melanoma||Rare||
| [[Composite melanoma]]||Rare||
*Melanoma that develops in proximity to other pre-existing epithelial malignancies (e.g. basal/squamous cell carcinoma)
*[[Melanoma]] that develops in the proximity of other pre-existing [[Epithelium|epithelial]] [[Cancer|malignancies]] (e.g. [[Basal cell carcinoma|basal]]/[[squamous cell carcinoma]])
*May be characterized by one of the following:
*May be characterized by one of the following:
::*Collision tumor: Collision of melanoma and another nearby malignant tumor
::*Collision [[tumor]]: Collision of [[melanoma]] and another nearby [[malignant]] [[tumor]]
::*Colonization: Colonization of melanocytes in a tumor
::*Colonization: Colonization of [[Melanocyte|melanocytes]] in a [[tumor]]
::*Combined: Two distinct tumors appear to have mixed features of the melanoma and the other tumor
::*Combined: Two distinct [[Tumor|tumors]] appear to have mixed features of the [[melanoma]] and the other [[tumor]]
::*Biphenotypic: One tumor that has features of melanoma and another epithelial malignancy
::*[[Biphenotypic melanoma|Biphenotypic]]: One [[tumor]] that has features of [[melanoma]] and another [[Epithelium|epithelial]] [[Cancer|malignancy]]
|}
|}



Latest revision as of 01:44, 2 January 2019

Melanoma Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Melanoma from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Melanoma classification On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Melanoma classification

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Melanoma classification

CDC on Melanoma classification

Melanoma classification in the news

Blogs on Melanoma classification

Directions to Hospitals Treating Melanoma

Risk calculators and risk factors for Melanoma classification

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Yazan Daaboul, M.D.; Serge Korjian M.D.

Overview

Melanoma may be classified into either cutaneous or non-cutaneous melanomas. The most common 4 sub-types of cutaneous melanoma include superficial spreading melanoma, nodular melanoma, acral lentiginous melanoma, and lentigo maligna melanoma. Less common sub-types of melanoma include desmoplastic/spindle cell melanoma, nevoid melanoma, spitzoid melanocytic melanoma, angiotropic melanoma, blue nevus-like melanoma, and composite melanoma.

Classification of Melanoma

Shown below is a table that demonstrates the various sub-classes of melanoma:[1][2]

Subtype Frequency Clinical Features
Common Subtypes
Superficial spreading melanoma 70%
  • Most common sub-type
  • Usually affects sun exposed sites among both men and women aged 50-70 years
  • Characterized by the presence of abundant junctional intra-epidermal spread of malignant melanocytes
Nodular melanoma 15-25%
  • Second most common subtype
  • Usually affects sun exposed sites among both men and women aged 50-70 years
  • Characterized by the absence of junctional intra-epidermal spread of malignant melanocytes
Acral lentiginous melanoma 5%
Lentigo maligna melanoma 1-5%
Non-cutaneous melanoma 5%
Less Common Subtypes
Desmoplastic/Spindle cell melanoma Rare
  • Lesion typically amelanotic and has a morphology similar to a scar tissue
  • Appears indolent but is highly infiltrative
  • Characterized by local recurrence and perineural spread
  • Usually affects males aged 60-70 years in sun exposed sites
  • May be de novo or can be associated with a pre-existing melanoma
  • Has several subtypes:
Nevoid melanoma Rare
Spitzoid melanocytic neoplasm Rare
Angiotropic melanoma Rare
Blue nevus-like melanoma Rare
  • Melanoma that develops from a pre-existing blue nevus
  • One of the rarest forms of melanoma
  • Appears as a blue nevus that has recently been rapidly expanding with irregular contours
  • Typically affects middle-aged men
Composite melanoma Rare

References

  1. Schanderdorf D, Kochs C, Livingstone E (2013). Handbook of Cutaneous Melanoma: A Guide to Diagnosis and Treatment. Springer.
  2. Mooi W, Krausz T (2007). Pathology of Melanocytic Disorders 2nd Ed. CRC Press.

Template:WH Template:WS