Kaposi's sarcoma: Difference between revisions
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==Background== | ==Background== | ||
* | {{Skin anatomy background images}} | ||
*Different classifications of Kaposi’s sarcoma based on patient population | |||
*Associated with [[HHV-8]] | |||
*Most common cancer in [[HIV]]/[[AIDS]] patients | |||
*Kaposi’s Sarcoma can be unmasked or induced by initiation of steroids or HAART | |||
*Cutaneous lower extremity lesions most common presentation | |||
*Kaposi’s sarcoma is an AIDS-defining illness | |||
*Treat with HAART and/or chemo | |||
=== | ===History=== | ||
*First described by Hungarian Dr. Moritz Kaposi in 1872; rare until 1980s with emergence of HIV/AIDS (1981 cluster of Kaposi’s sarcoma in young men in NYC and California; 1982 listed as AIDS-defining illness by CDC) | |||
*Human Herpesvirus 8 (HHV8) | |||
**Large, double-stranded DNA virus | |||
**Necessary but NOT sufficient to cause disease | |||
**Also associated with body-cavity based lymphomas, multicentric Castleman’s disease (angiofollicular lymph node hyperplasia) | |||
===Classifications=== | |||
*Classic Kaposi’s (CK) | |||
**Indolent, chronic form, rarely disseminated | |||
**Skin most commonly effected, lower extremities | |||
**~3:1 Male:Female, Age > 60 years old with Mediterranean, Eastern European or Middle Eastern origin | |||
*Endemic Kaposi’s sarcoma (Africa) | |||
**Male adults or children of both sexes | |||
**Equatorial/Sub-Saharan Africa | |||
**Aggressive form with lymph node involvement (lymphedema) | |||
**27%, 35%, and 24% of total cancer burden in Uganda, Zimbabwe and Mozambique, respectively | |||
*AIDS-KS | |||
**Developed countries: Men who have sex with men | |||
**Developing countries: Heterosexual men and women (Africa) | |||
**Aggressive disease – most commonly in lungs, gastrointestinal tract, mouth, and genitalia | |||
**Most common cancer in HIV/AIDS patients | |||
*Iatrogenic due to immunosuppression – Most commonly organ transplant-associated | |||
**Increased risk after solid organ transplantation | |||
**Transplant itself may transmit HHV-8 infection | |||
**Male > Female (3.3:1), average age 43 yo | |||
**Cutaneous lesion presentation most common | |||
**More common in liver than kidney transplant patients | |||
*Immune Reconstitution Inflammatory Syndrome (IRIS) Phenomenon | |||
**Initiation of retroviral therapy can cause the development of KS | |||
**True unmasked KS-IRIS begins within 6 months of initiating therapy, and the rates remain unclear | |||
==Clinical Features== | ==Clinical Features== | ||
[[File:Kaposis sarcoma 01.jpg|thumb|Kaposi sarcoma. Characteristic purple lesions on the nose in an HIV-positive female.]] | |||
[[File:Kaposis Sarcoma Lesions.jpg|thumb|Kaposi's sarcoma skin lesion]] | |||
[[File:Patch stage Kaposi's sarcoma.jpg|thumb|Patch stage Kaposi's sarcoma. Red to brownish irregularly shaped macules and plaques.]] | |||
[[File:Kaposi’s sarcoma intraoral AIDS 072 lores.jpg|thumb|An HIV-positive person presenting with a Kaposi's sarcoma lesion with an overlying candidiasis infection in their mouth.]] | |||
*[[rash|Cutaneous]] | |||
*Heterogeneous appearance | |||
**Color – dark blue, reddish, purple, violaceous, dark brown/black | |||
**Location – extremities, most commonly the feet | |||
**Lesions: macules, plaques, nodules | |||
**Associated [[lymphedema]] | |||
*Pulmonary | |||
**Gradual Onset (2-4 weeks) | |||
**[[Cough]] | |||
**[[Dyspnea]] | |||
**[[Fever]] | |||
**[[Hemoptysis]] | |||
**Asymptomatic | |||
*Gastrointestinal | |||
**[[GI bleed|Bleeding]] | |||
**[[SBO|Obstruction]] | |||
==Differential Diagnosis== | ==Differential Diagnosis== | ||
* | *Cutaneous Lesions: | ||
**Bacillary angiomatosis | |||
**[[Purpura]] | |||
**Hematomas | |||
**Angiomas | |||
**Dermatofibromas | |||
**Nevi | |||
*Pulmonary Lesions in HIV/AIDs: | |||
**Bacterial [[pneumonia]] | |||
**[[PCP pneumonia|PCP]] | |||
**[[TB]] | |||
**[[Fungal infections]] | |||
*Anorectal Lesions in HIV/AIDs: | |||
**Common: [[Anal fissure]], [[perianal abscess|abscess]] and/or fistula, [[hemorrhoid]], [[pilonidal cyst|[pilonidal disease]] | |||
**STDs: [[Gonorrhea]], [[chlamydia]], [[HSV|herpes]], [[chancroid]], [[syphilis]], [[condyloma acuminata]] | |||
**Infectious: [[TB]], [[CMV]] infection, [[actinomyces|actinomycosis]], [[cryptococcosis]] | |||
**Neoplastic: [[Lymphoma]], [[Kaposi’s sarcoma]], [[squamous cell carcinoma]] | |||
==Diagnosis== | {{HIV associated conditions}} | ||
{{DDX dark raised lesions}} | |||
==Evaluation== | |||
*Clinical impression | |||
*Biopsy is gold standard for definitive diagnosis | |||
*WHO Clinical Staging of HIV/AIDS | |||
**Stage 4: Presumptive Diagnosis of HIV/AIDS can be made from clinical signs of Kaposi’s | |||
*GI manifestations | |||
**Unlikely visible on XR; can be seen on flex sig or colonoscopy | |||
*Pulmonary Manifestations | |||
**Heterogeneous on [[CXR]] - nodular, interstitial and/or alveolar infiltrates, pleural effusion, hilar and/or mediastinal adenopathy, or an isolated nodule | |||
===Staging=== | |||
*Classic Kaposi's Sarcoma | |||
**No staging system. It is excluded in TNM Staging of soft tissue sarcomas by American Joint Committee on Cancer (AJCC) | |||
*AIDS-KS Staging | |||
{| {{table}} | |||
| align="center" style="background:#f0f0f0;"|''' ''' | |||
| align="center" style="background:#f0f0f0;"|'''Good Risk (all of the following)''' | |||
| align="center" style="background:#f0f0f0;"|'''Poor Risk (any of the following)''' | |||
|- | |||
| Tumor, T||T0: Skin and/or lymph nodes and/or minimal oral disease||TI: Tumor-associated edema or ulceration, extensive oral KS, GI KS, KS in other non-nodal viscera | |||
|- | |||
| Immune System, I||CD4 > 200||CD4 < 200 | |||
|- | |||
| Systemic Illness, S||S0: No history of OI or thrust, No "B" Symptoms (fever, night sweats, weight loss, diarrhea > 2 weeks) Karnofsky performance > 70||SI: History of OI and/or thrush, "B" symptoms, Karnofsky performance <70, Other HIV-related illness | |||
|- | |||
|} | |||
==Management== | ==Management== | ||
*Highly Active Anti-retroviral therapy (HAART): | |||
**Can achieve remission in 60-90% remission in stage T0 disease | |||
**Can combine with chemotherapy | |||
*Chemotherapy: | |||
**First-line: Pegylated liposomal doxorubicin (PLD) 20mg/m2 every three weeks (unless cardiac contraindication) | |||
**Second-line: Vinblastine, Bleomycin, Paclitaxel, Etoposide, Gemcitabine | |||
*Cutaneous Specific Treatment: | |||
**Alitretinoin (9-cis-retinoic acid) topical gel 0.1% FDA-approved for cutaneous AIDS-associated KS | |||
**Intralesion Injection: Vinblastine or Bleomycin or INF-alpha | |||
**Vinblastine 0.2 – 0.3mg/mL solution with a volume of 1 mL per 0.5 cm2 of lesion | |||
**IFNa - FDA approved for AIDS-associated KS | |||
*Radiation Therapy | |||
**30 Gy in 15 daily 2 Gy fractions | |||
*Other Drug Trials: | |||
**Bevacizumab - an anti-VEGF-A | |||
**Imatinib - monoclonal antibody tyrosine kinase receptor | |||
*[[Steroids]] | |||
**Associated with generation and exacerbation of KS | |||
**Important implications because of the high use of steroids in this patient population (HIV/AIDS, transplant) | |||
**Once steroids are removed, KS can regress | |||
==See Also== | ==See Also== | ||
*[[HIV - AIDS (Main)]] | |||
==External Links== | ==External Links== | ||
*http://www.ncbi.nlm.nih.gov/pubmed/25256409 | |||
*http://www.ncbi.nlm.nih.gov/pubmed/20413015 | |||
== | ==References== | ||
*Farge, D. "Kaposi's Sarcoma in Organ Transplant Recipients. The Collaborative Transplantation Research Group of Ile De France." The European Journal of Medicine 2.6 (1993): 339-43. | |||
*Fenig, Eyal, Baruch Brenner, Erica Rakowsky, Moshe Lapidoth, Alan Katz, and Aaron Sulkes. "Classic Kaposi Sarcoma." American Journal of Clinical Oncology 21.5 (1998): 498-500. | |||
*Krown, SE, C. Metroka, and JC Wemz. "Kaposi's Sarcoma in the Acquired Immune Deficiency Syndrome: A Proposal for Uniform Evaluation, Response and Staging Criteria." Journal of Clinical Oncology 7.9 (1989): 1201-207. | |||
*Krown, SE, MA Testa, and J. Huang. "AIDS-related Kaposi's Sarcoma: Prospective Validation of the AIDS Clinical Trials Group Staging Classification. AIDS Clinical Trials Group Oncology Committee." Journal of Clinical Oncology 15.9 (1997): 3085-092. | |||
*Moosa, M.r. "Kaposi's Sarcoma in Kidney Transplant Recipients: A 23-year Experience." QJM 98.3 (2005): 205-14. | |||
*Osawa, R., N. Kato, T. Yanagi, and N. Yamane. "Clearance of Recurrent, Classical Kaposi’s Sarcoma Using Multiple Paclitaxel Treatments." Acta Derm Venereol Acta Dermato-Venereologica 87.5 (2007): 435-36. Web. | |||
*Robey, Rebecca C., and Mark Bower. "Facing up to the Ongoing Challenge of Kaposiʼs Sarcoma." Current Opinion in Infectious Diseases 28.31 (2015). | |||
*Rosen, Peter, and John A. Marx. Rosen's Emergency Medicine: Concepts and Clinical Practice. 8th ed. Philadelphia: Elsevier Saunders, 2014. | |||
*Safai, B., and R. A. Good. "Kaposi's Sarcoma: A Review and Recent Developments." CA: A Cancer Journal for Clinicians 31.1 (1981): 2-12. | |||
[[Category: | [[Category:Dermatology]] | ||
[[Category:ID]] | [[Category:ID]] | ||
Latest revision as of 16:36, 11 December 2024
Background
- Different classifications of Kaposi’s sarcoma based on patient population
- Associated with HHV-8
- Most common cancer in HIV/AIDS patients
- Kaposi’s Sarcoma can be unmasked or induced by initiation of steroids or HAART
- Cutaneous lower extremity lesions most common presentation
- Kaposi’s sarcoma is an AIDS-defining illness
- Treat with HAART and/or chemo
History
- First described by Hungarian Dr. Moritz Kaposi in 1872; rare until 1980s with emergence of HIV/AIDS (1981 cluster of Kaposi’s sarcoma in young men in NYC and California; 1982 listed as AIDS-defining illness by CDC)
- Human Herpesvirus 8 (HHV8)
- Large, double-stranded DNA virus
- Necessary but NOT sufficient to cause disease
- Also associated with body-cavity based lymphomas, multicentric Castleman’s disease (angiofollicular lymph node hyperplasia)
Classifications
- Classic Kaposi’s (CK)
- Indolent, chronic form, rarely disseminated
- Skin most commonly effected, lower extremities
- ~3:1 Male:Female, Age > 60 years old with Mediterranean, Eastern European or Middle Eastern origin
- Endemic Kaposi’s sarcoma (Africa)
- Male adults or children of both sexes
- Equatorial/Sub-Saharan Africa
- Aggressive form with lymph node involvement (lymphedema)
- 27%, 35%, and 24% of total cancer burden in Uganda, Zimbabwe and Mozambique, respectively
- AIDS-KS
- Developed countries: Men who have sex with men
- Developing countries: Heterosexual men and women (Africa)
- Aggressive disease – most commonly in lungs, gastrointestinal tract, mouth, and genitalia
- Most common cancer in HIV/AIDS patients
- Iatrogenic due to immunosuppression – Most commonly organ transplant-associated
- Increased risk after solid organ transplantation
- Transplant itself may transmit HHV-8 infection
- Male > Female (3.3:1), average age 43 yo
- Cutaneous lesion presentation most common
- More common in liver than kidney transplant patients
- Immune Reconstitution Inflammatory Syndrome (IRIS) Phenomenon
- Initiation of retroviral therapy can cause the development of KS
- True unmasked KS-IRIS begins within 6 months of initiating therapy, and the rates remain unclear
Clinical Features
- Cutaneous
- Heterogeneous appearance
- Color – dark blue, reddish, purple, violaceous, dark brown/black
- Location – extremities, most commonly the feet
- Lesions: macules, plaques, nodules
- Associated lymphedema
- Pulmonary
- Gradual Onset (2-4 weeks)
- Cough
- Dyspnea
- Fever
- Hemoptysis
- Asymptomatic
- Gastrointestinal
Differential Diagnosis
- Cutaneous Lesions:
- Bacillary angiomatosis
- Purpura
- Hematomas
- Angiomas
- Dermatofibromas
- Nevi
- Pulmonary Lesions in HIV/AIDs:
- Bacterial pneumonia
- PCP
- TB
- Fungal infections
- Anorectal Lesions in HIV/AIDs:
- Common: Anal fissure, abscess and/or fistula, hemorrhoid, [pilonidal disease
- STDs: Gonorrhea, chlamydia, herpes, chancroid, syphilis, condyloma acuminata
- Infectious: TB, CMV infection, actinomycosis, cryptococcosis
- Neoplastic: Lymphoma, Kaposi’s sarcoma, squamous cell carcinoma
HIV associated conditions
- HIV neurologic complications
- HIV pulmonary complications
- Ophthalmologic complications
- Other
- HAART medication side effects[1]
- HAART-induced lactic acidosis
- Neuropyschiatric effects
- Hepatic toxicity
- Renal toxicity
- Steven-Johnson's
- Cytopenias
- GI symptoms
- Endocrine abnormalities
Dark raised skin lesions
Evaluation
- Clinical impression
- Biopsy is gold standard for definitive diagnosis
- WHO Clinical Staging of HIV/AIDS
- Stage 4: Presumptive Diagnosis of HIV/AIDS can be made from clinical signs of Kaposi’s
- GI manifestations
- Unlikely visible on XR; can be seen on flex sig or colonoscopy
- Pulmonary Manifestations
- Heterogeneous on CXR - nodular, interstitial and/or alveolar infiltrates, pleural effusion, hilar and/or mediastinal adenopathy, or an isolated nodule
Staging
- Classic Kaposi's Sarcoma
- No staging system. It is excluded in TNM Staging of soft tissue sarcomas by American Joint Committee on Cancer (AJCC)
- AIDS-KS Staging
| Good Risk (all of the following) | Poor Risk (any of the following) | |
| Tumor, T | T0: Skin and/or lymph nodes and/or minimal oral disease | TI: Tumor-associated edema or ulceration, extensive oral KS, GI KS, KS in other non-nodal viscera |
| Immune System, I | CD4 > 200 | CD4 < 200 |
| Systemic Illness, S | S0: No history of OI or thrust, No "B" Symptoms (fever, night sweats, weight loss, diarrhea > 2 weeks) Karnofsky performance > 70 | SI: History of OI and/or thrush, "B" symptoms, Karnofsky performance <70, Other HIV-related illness |
Management
- Highly Active Anti-retroviral therapy (HAART):
- Can achieve remission in 60-90% remission in stage T0 disease
- Can combine with chemotherapy
- Chemotherapy:
- First-line: Pegylated liposomal doxorubicin (PLD) 20mg/m2 every three weeks (unless cardiac contraindication)
- Second-line: Vinblastine, Bleomycin, Paclitaxel, Etoposide, Gemcitabine
- Cutaneous Specific Treatment:
- Alitretinoin (9-cis-retinoic acid) topical gel 0.1% FDA-approved for cutaneous AIDS-associated KS
- Intralesion Injection: Vinblastine or Bleomycin or INF-alpha
- Vinblastine 0.2 – 0.3mg/mL solution with a volume of 1 mL per 0.5 cm2 of lesion
- IFNa - FDA approved for AIDS-associated KS
- Radiation Therapy
- 30 Gy in 15 daily 2 Gy fractions
- Other Drug Trials:
- Bevacizumab - an anti-VEGF-A
- Imatinib - monoclonal antibody tyrosine kinase receptor
- Steroids
- Associated with generation and exacerbation of KS
- Important implications because of the high use of steroids in this patient population (HIV/AIDS, transplant)
- Once steroids are removed, KS can regress
See Also
External Links
References
- Farge, D. "Kaposi's Sarcoma in Organ Transplant Recipients. The Collaborative Transplantation Research Group of Ile De France." The European Journal of Medicine 2.6 (1993): 339-43.
- Fenig, Eyal, Baruch Brenner, Erica Rakowsky, Moshe Lapidoth, Alan Katz, and Aaron Sulkes. "Classic Kaposi Sarcoma." American Journal of Clinical Oncology 21.5 (1998): 498-500.
- Krown, SE, C. Metroka, and JC Wemz. "Kaposi's Sarcoma in the Acquired Immune Deficiency Syndrome: A Proposal for Uniform Evaluation, Response and Staging Criteria." Journal of Clinical Oncology 7.9 (1989): 1201-207.
- Krown, SE, MA Testa, and J. Huang. "AIDS-related Kaposi's Sarcoma: Prospective Validation of the AIDS Clinical Trials Group Staging Classification. AIDS Clinical Trials Group Oncology Committee." Journal of Clinical Oncology 15.9 (1997): 3085-092.
- Moosa, M.r. "Kaposi's Sarcoma in Kidney Transplant Recipients: A 23-year Experience." QJM 98.3 (2005): 205-14.
- Osawa, R., N. Kato, T. Yanagi, and N. Yamane. "Clearance of Recurrent, Classical Kaposi’s Sarcoma Using Multiple Paclitaxel Treatments." Acta Derm Venereol Acta Dermato-Venereologica 87.5 (2007): 435-36. Web.
- Robey, Rebecca C., and Mark Bower. "Facing up to the Ongoing Challenge of Kaposiʼs Sarcoma." Current Opinion in Infectious Diseases 28.31 (2015).
- Rosen, Peter, and John A. Marx. Rosen's Emergency Medicine: Concepts and Clinical Practice. 8th ed. Philadelphia: Elsevier Saunders, 2014.
- Safai, B., and R. A. Good. "Kaposi's Sarcoma: A Review and Recent Developments." CA: A Cancer Journal for Clinicians 31.1 (1981): 2-12.
- ↑ Gutteridge, David L MD, MPH, Egan, Daniel J. MD. The HIV-Infected Adult Patient in The Emergency Department: The Changing Landscape of the Disease. Emergency Medicine Practice: An Evidence-Based Approach to Emergency Medicine. Vol 18, Num 2. Feb 2016.
