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MELANOMA-ANAL CANAL
Dr.A.Joseph Stalin Mch PG
PROF.DR.R.RAJARAMAN’S UNIT
DEPT OF SURGICAL ONCOLOGY
GOVT ROYAPETTAH HOSPITAL
CHENNAI
CONTENTS
• Anal Mucosal Melanoma
- Introduction
- Clinical presentation
- Diagnosis
- Treatment
.Take home message
INTRODUCTION
• Anal melanoma - 0.5 to 2% - anal malignancies
• Less than 2% of all melanomas.
• The third most common melanoma after the
cutaneous and ocular varieties.
• Most common site for primary gastrointestinal
melanoma.
ETIOLOGY
• No known risk factors.
• Risk factors for cutaneous melanoma like
nevus, sunlight exposure does not predispose
to anal melanoma.
PATHOLOGY
• Melanoma arises from melanocytes derived
from neural crest cells.
• Melanocytes subjected to carcinogenic stimuli
undergo malignant transformation.
• Carcinogenic stimuli in anal melanoma unknown
• Subsets of anal melanoma shows mutation in
BRAF, Ckit , p53 mutation.
Symptoms
• Bleeding per rectum –
most common (50-
60%)
• Perianal itching and
irritation (15-20%)
• mass protruding through
anus.
• perianal discharge.
CLINICAL PRESENTATION
• More common in women
• Mean age :70 yrs(29-91)
• Distant metastasis seen in 30% of people at
diagnosis
SPREAD
• Lymphatic Spread : Inguinal & mesorectal
nodes.
• Systemic : Lung,Liver,Brain , Bone
DIAGNOSIS
• Diagnosis can be made with visual inspection and
anoscopy.
• commonly present as polypoidal mass
• Distance from anal verge and mobility assessed
• Clinically evident pigmented leision only in
20 % of cases.In others pigmentation is
obscured.
• 20 % are amelanotic histologically.
THROMBOSED PILE LIKE MASSS
Polypoidal lesion in colonoscopy
DIFFERENTIAL DIAGNOSIS
●Anal carcinoma/lymphoma
●Perianal haematoma
●Thrombosed haemorrhoids
●Anal or Rectal Polyp
INVESTIGATIONS
• PROCTOSCOPY & BIOPSY
• USG ABDOMEN/PELVIS
• ENDOLUMINAL USG
• PET ?
● USG abdomen/pelvis : to r/o liver mets.
● ENDOLUMINAL USG : Depth of invasion
and nodal status.
ROLE OF PET CT
• Positron emission tomography (PET) may be
helpful for staging of anorectal melanoma.
• The sensitivity was 74 to 100% and specificity
67 to 100%.
IMMUNOHISTOCHEMISTRY
Melanoma panel of markers
S-100 protein
Vimentin,
Melan-A,
HMB-45.
To R/o other disease
*Cytokeratins (Paget’s disease), CD45 (lymphoma),
chromogranin and synaptophysin (undifferen-
tiated carcinoma), CD34 (GIST) and Desmin and
caldesmon (sarcoma)
STAGING
• The staging of anal melanoma differs from that of
cutaneous melanoma( based on Breslow
classification).
• Anal melanoma is staged on a clinical basis, focusing on
locoregional and distant spread.
( Clinics of Colorectal surgery vol19 Ross etal )
• Stage I is local disease.
• stage II is local disease with regional lymph nodes.
• stage III is distant metastatic disease.
STAGE I & II
• Surgical excision is the treatment of choice.
• Melanoma is highly resistant to RT/ Chemo.
No role either as defnitive treatment or as
adjuvant therapy.
SURGERY
• WIDE LOCAL EXCISION / ABDOMINO PERINEAL
RESECTION for Stage I/II disease
• Wide local excision (R0 resection ) is
preferred.
WIDE LOCAL EXCISION
• Loan star retractor preferred.
• 1 cm margin(R0 resection) .
• TEMS for localised leision in rectum
APR
• When anal sphinter is involved or R0
resection mandates sphinter excision, APR
indicated in stage I& II.
• No survival advantage for APR when
compared to wide local excision
STUDIES
• Droesh et al -2005
• 301 pt
• 172-APR,129- WLE.
• Mean survival same for both.
• A comparison of wide local excision with
abdominoperineal resection in anorectal melanoma.
• Yap LB1, Neary P.
• Seventeen large case series from over the past 10
years were reviewed.
• Comparison of the survival of patients who underwent
APR with those who underwent WLE showed no
statistically significant advantage for either procedure
in patients at all disease stages.
• APR should therefore only be performed when local
excision is not possible or for palliative purposes.
Role of lymph node dissection
• Lymph node dissection – inguinal/mesorectal-
does not confer survival advantage although it
improves locoregional control.
• Bollo et al(23 patients )
• Moozar et al (14 patients )
• Brady et al(retrospective analysis )
STAGE III
• Systemic chemotherapy
• Drugs used are akin to cutaneous melanoma
• Commonly used drugs
Dacarbazine
Temozolamide
TARGETED THERAPY
• cKIT/ BRAF mutation seen in some subgroup
• Targeted therapy –cKIT ( Imatinib)/ BRAF
(Verufunamib) in adjuvant and metastatic
setting shows good response in phase II trial.
• Yeh et al .Interim analysis shows median
survival improves by 3-5 months.
PROGNOSTIC FACTORS
• Tumour thickness.
• Ulceration
• Mitotic rate
• Nodal involvement.
• Relation to dentate line.
PROGNOSIS
• STAGE I &II : mean survival 11 – 20 months.
• STAGE III : Less than 10 months.
TAKE HOME MESSAGE
• Anal melanoma is a rare and aggressive
variant of mucosal melanoma
• Often misdiagnosed as benign leision.
• High index of suspicion is needed.
• Immunohistochemistry is the gold standard
for diagnosis.
• Surgery is the treatment of choice for stage
I& II .
• Wide local excision is the preferred surgery.
• Role of targeted therapy is emerging.
• Mean survival is only 20 months
THANK U

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Melanoma anal canal

  • 1. MELANOMA-ANAL CANAL Dr.A.Joseph Stalin Mch PG PROF.DR.R.RAJARAMAN’S UNIT DEPT OF SURGICAL ONCOLOGY GOVT ROYAPETTAH HOSPITAL CHENNAI
  • 2. CONTENTS • Anal Mucosal Melanoma - Introduction - Clinical presentation - Diagnosis - Treatment .Take home message
  • 3. INTRODUCTION • Anal melanoma - 0.5 to 2% - anal malignancies • Less than 2% of all melanomas. • The third most common melanoma after the cutaneous and ocular varieties. • Most common site for primary gastrointestinal melanoma.
  • 4. ETIOLOGY • No known risk factors. • Risk factors for cutaneous melanoma like nevus, sunlight exposure does not predispose to anal melanoma.
  • 5. PATHOLOGY • Melanoma arises from melanocytes derived from neural crest cells. • Melanocytes subjected to carcinogenic stimuli undergo malignant transformation. • Carcinogenic stimuli in anal melanoma unknown • Subsets of anal melanoma shows mutation in BRAF, Ckit , p53 mutation.
  • 6. Symptoms • Bleeding per rectum – most common (50- 60%) • Perianal itching and irritation (15-20%) • mass protruding through anus. • perianal discharge.
  • 7. CLINICAL PRESENTATION • More common in women • Mean age :70 yrs(29-91) • Distant metastasis seen in 30% of people at diagnosis
  • 8. SPREAD • Lymphatic Spread : Inguinal & mesorectal nodes. • Systemic : Lung,Liver,Brain , Bone
  • 9. DIAGNOSIS • Diagnosis can be made with visual inspection and anoscopy. • commonly present as polypoidal mass • Distance from anal verge and mobility assessed
  • 10. • Clinically evident pigmented leision only in 20 % of cases.In others pigmentation is obscured. • 20 % are amelanotic histologically.
  • 12. Polypoidal lesion in colonoscopy
  • 13. DIFFERENTIAL DIAGNOSIS ●Anal carcinoma/lymphoma ●Perianal haematoma ●Thrombosed haemorrhoids ●Anal or Rectal Polyp
  • 14. INVESTIGATIONS • PROCTOSCOPY & BIOPSY • USG ABDOMEN/PELVIS • ENDOLUMINAL USG • PET ?
  • 15. ● USG abdomen/pelvis : to r/o liver mets. ● ENDOLUMINAL USG : Depth of invasion and nodal status.
  • 16. ROLE OF PET CT • Positron emission tomography (PET) may be helpful for staging of anorectal melanoma. • The sensitivity was 74 to 100% and specificity 67 to 100%.
  • 17. IMMUNOHISTOCHEMISTRY Melanoma panel of markers S-100 protein Vimentin, Melan-A, HMB-45. To R/o other disease *Cytokeratins (Paget’s disease), CD45 (lymphoma), chromogranin and synaptophysin (undifferen- tiated carcinoma), CD34 (GIST) and Desmin and caldesmon (sarcoma)
  • 18. STAGING • The staging of anal melanoma differs from that of cutaneous melanoma( based on Breslow classification). • Anal melanoma is staged on a clinical basis, focusing on locoregional and distant spread. ( Clinics of Colorectal surgery vol19 Ross etal ) • Stage I is local disease. • stage II is local disease with regional lymph nodes. • stage III is distant metastatic disease.
  • 19. STAGE I & II • Surgical excision is the treatment of choice. • Melanoma is highly resistant to RT/ Chemo. No role either as defnitive treatment or as adjuvant therapy.
  • 20. SURGERY • WIDE LOCAL EXCISION / ABDOMINO PERINEAL RESECTION for Stage I/II disease • Wide local excision (R0 resection ) is preferred.
  • 21. WIDE LOCAL EXCISION • Loan star retractor preferred. • 1 cm margin(R0 resection) . • TEMS for localised leision in rectum
  • 22. APR • When anal sphinter is involved or R0 resection mandates sphinter excision, APR indicated in stage I& II. • No survival advantage for APR when compared to wide local excision
  • 23. STUDIES • Droesh et al -2005 • 301 pt • 172-APR,129- WLE. • Mean survival same for both.
  • 24. • A comparison of wide local excision with abdominoperineal resection in anorectal melanoma. • Yap LB1, Neary P. • Seventeen large case series from over the past 10 years were reviewed. • Comparison of the survival of patients who underwent APR with those who underwent WLE showed no statistically significant advantage for either procedure in patients at all disease stages. • APR should therefore only be performed when local excision is not possible or for palliative purposes.
  • 25. Role of lymph node dissection • Lymph node dissection – inguinal/mesorectal- does not confer survival advantage although it improves locoregional control. • Bollo et al(23 patients ) • Moozar et al (14 patients ) • Brady et al(retrospective analysis )
  • 26. STAGE III • Systemic chemotherapy • Drugs used are akin to cutaneous melanoma • Commonly used drugs Dacarbazine Temozolamide
  • 27. TARGETED THERAPY • cKIT/ BRAF mutation seen in some subgroup • Targeted therapy –cKIT ( Imatinib)/ BRAF (Verufunamib) in adjuvant and metastatic setting shows good response in phase II trial. • Yeh et al .Interim analysis shows median survival improves by 3-5 months.
  • 28. PROGNOSTIC FACTORS • Tumour thickness. • Ulceration • Mitotic rate • Nodal involvement. • Relation to dentate line.
  • 29. PROGNOSIS • STAGE I &II : mean survival 11 – 20 months. • STAGE III : Less than 10 months.
  • 30. TAKE HOME MESSAGE • Anal melanoma is a rare and aggressive variant of mucosal melanoma • Often misdiagnosed as benign leision. • High index of suspicion is needed. • Immunohistochemistry is the gold standard for diagnosis.
  • 31. • Surgery is the treatment of choice for stage I& II . • Wide local excision is the preferred surgery. • Role of targeted therapy is emerging. • Mean survival is only 20 months