Ulcers - ASCCP

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Ulcers Aruna Venkatesan, MD Associate Chief of Dermatology Director of Genital Dermatology Clinic Santa Clara Valley Medical Center (SCVMC) Associate Professor of Dermatology, Affiliated Stanford University

Transcript of Ulcers - ASCCP

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Ulcers

Aruna Venkatesan, MD

Associate Chief of Dermatology

Director of Genital Dermatology Clinic

Santa Clara Valley Medical Center (SCVMC)

Associate Professor of Dermatology, Affiliated

Stanford University

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Disclosures

No financial relationships or conflict of interest to disclose

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Learning Objectives

At the end of this lecture, the participant will gain knowledge on the:

• Definition of an ulcer

• Differential diagnosis of an ulcer

• Evaluation of ulcers

• Treatment strategies for ulcers

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Recommended References

• Pipkin C. Erosive Diseases of the Vulva. Dermatol Clin. 2010 Oct;28(4):737-52.

• Bandow GD. Diagnosis and Management of Vulvar Ulcers. Dermatol Clin. 2010 Oct;28(4):753-64.

• Black M et al. Obstetric and Gynecologic Dermatology, 3rd Edition. Elsevier Limited, 2008.

• Edwards L and PJ Lynch, eds. Genital Dermatology Atlas, 2nd Edition. Philadelphia: Lippincott Williams & Wilkins, 2011.

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Outline

• An exam finding not a diagnosis

• Ulcer vs. erosion

• Differential diagnosis

• Approach to evaluation• Physical exam• Other diagnostic tools

• Specific diagnoses• HSV• Aphthous ulcers• Pemphigus vulgaris

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Outline

• An exam finding not a diagnosis

• Ulcer vs. erosion

• Differential diagnosis

• Approach to evaluation• Physical exam• Other diagnostic tools

• Specific diagnoses• HSV• Aphthous ulcers• Pemphigus vulgaris

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Ulcer

• An exam finding not a diagnosis

• Many different causes

• Use your exam, labs, studies to narrow down diagnosis

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Outline

• An exam finding not a diagnosis

• Ulcer vs. erosion

• Differential diagnosis

• Approach to evaluation• Physical exam• Other diagnostic tools

• Specific diagnoses• HSV• Aphthous ulcers• Pemphigus vulgaris

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Ulcer vs. Erosion

• Erosion• Partial to complete loss of epidermis y• Doesn’t penetrate through basement membra e• Red base• Heals without scaring

• Ulcer• Full thickness epidermal loss + penetration through

basement membrane to dermis • Usually yellow-white base• Heals with scarring

https://en.wikipedia.org/wiki/Skin_fissure

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Ulcer vs. Erosion

• Important or Nitpicky?

• Important!• Exam findings are different

• Differential https://en.wikipedia.org/wiki/Skin_fissure

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Outline

• An exam finding not a diagnosis

• Ulcer vs. erosion

• Differential diagnosis

• Approach to evaluation• Physical exam• Other diagnostic tools

• Specific diagnoses• HSV• Aphthous ulcers• Pemphigus vulgaris

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Differential Diagnosis

• Ulcer = morphology

• Differential diagnosis is broad• Infectious

• Inflammatory

• Neoplastic

• ‘Outside Job’

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Differential Diagnosis-- Infectious• Viral

• Herpes simplex virus (esp. if immunocompromised host)

• Herpes zoster virus

• Cytomegalovirus

• Bacterial

• Ecthyma (gram positive or gram negative)

• Granuloma inguinale

• Chancroid

• Lymphogranuloma venereum (LGV)

• Treponemal

• Primary syphilis

• Fungal

• Angioinvasive fungi

• Mycobacterial

• Tuberculosis

• Atypical mycobacterial

• Parasitic

• Amebiasis

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Differential Diagnosis-- Inflammatory

• Aphthae• Behçet’s disease

• Pyoderma gangrenosum

• Crohn’s disease

• Hailey-Hailey disease (benign familial pemphigus)

• Autoimmune blistering disease• Pemphigus vulgaris• Bullous pemphigoid• Cicatricial pemphigoid• Linear IgA disease• Bullous systemic lupus erythematosus• Epidermolysis bullosa acquisita

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Differential Diagnosis-- Inflammatory

• Aphthae• Behçet’s disease

• Pyoderma gangrenosum

• Crohn’s disease

• *Hailey-Hailey disease (benign familial pemphigus)

• *Autoimmune blistering disease Erosion versus ulcer Depth is important• Pemphigus vulgaris• Bullous pemphigoid• Cicatricial pemphigoid• Linear IgA disease• Bullous systemic lupus erythematosus• Epidermolysis bullosa acquisita

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Differential Diagnosis-- Neoplastic

• High Grade Squamous Intraepithelial Lesion (HSIL)/ Squamous Cell Carcinoma

• Basal Cell Carcinoma

• Melanoma

• Extramammary Paget’s disease

• Langerhans cell histiocytosis

• Others

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Differential Diagnosis– ‘Outside Job’• Drug

• Fixed drug eruption

• Stevens –Johnson syndrome / Toxic epidermal necrolysis (SJS/TEN)• Severe – life threatening

• 2+ mucous membranes involved

• Self-induced

• Diagnosis of exclusion

• Angular ulcers with scarring, dyspigmentation

• Full skin exam

• May have underlying drug use, psychiatric condition

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Approach to Evaluation-- Physical Exam• Oral exam (+ ROS)

• Remainder of skin

• Genital exam• Erosion vs. Ulcer

• Shape, distribution of lesions

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Approach to Evaluation– Other Diagnostic Tools • Blood Tests

• HIV 1, 2 Ab

• Syphilis screening test• Lab/hospital determines exam

• Syphilis EIA (treponemal test) more common

• Positive indicates history of exposure at some point (may be treated)

• Can have false negatives in primary syphilis

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Approach to Evaluation– Other Diagnostic Tools • Blood Tests

• CBC with differential and manual peripheral smear

• HSV Serologies

• Indirect Immunofluorescence

• TB Quantiferon

• Blood cultures

• Folate, B12, zinc, iron

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Approach to Evaluation– Other Diagnostic Tools • Swabs

• HSV/VZV

• Multiple tests available

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Approach to Evaluation– Other Diagnostic Tools • Others

• Colonoscopy

• CXR

• Referrals

• Collaborate with other specialties

• History

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Approach to Evaluation– Other Diagnostic Tools • History

• Ask questions, before and after tests

• Level of sickness (outpatient versus inpatient)

• E.g. May be more likely to biopsy, perform multiple studies in sick patient

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Approach to Evaluation– Other Diagnostic Tools • History

• Ask questions, before and after tests

• Drug history

• E.g. Acute onset conjunctival redness, oral and genital sores, dusky skin lesions 5 weeks after starting lamotrigine SJS/TEN

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Approach to Evaluation– Other Diagnostic Tools • History

• Ask questions, before and after tests

• Drug history

• E.g. Recurrent painful circular lesions on lips, vulva, skin after taking prn naproxen Fixed Drug Eruption

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HSV

• Classic herpetiform (grouped) vesicles on red base• In immunocompetent host

• Deep, expansive, multi-site ulcers• In immunocompromised host

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HSV in Immunocompromised Host

• High degree of clinical suspicion• HSV testing (DFA/culture/PCR)• HIV Ab testing• Biopsy for viral tissue culture• Biopsy for H&E, immunostain analysis

• Treatment• First, give treatment dose of anti-virals until fully healed• Then given ongoing suppressive dose• Valacyclovir (better bioavailability), Acyclovir (cheaper)

• If treatment fails, consider CMV co-infection or acyclovir resistance

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Aphthae

• Very common

• Oral, Genital

• ~20-60% of people have oral aphthae

• Painful red lesions with yellow-white fibrin base

• Cause unclear• Cell-mediated response to trauma, irritant, virus, bacteria?

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Common Acute Presentation• Adolescent girls (~9-18 y.o.)

• Viral prodrome (fever, sore throat, malaise)

• Very painful aphthae

• If severe, may be unable to urinate catheterization required

• Inflammation to viral trigger vs. infection?

• Workup generally focused• HSV swab (DFA/Culture/PCR)• HIV Ab• Syphilis screen

• Treat the inflammation • Severe: Prednisone 1mg/kg PO qam until pain resolves• Mild-mod: Topical clobetesol oint BID to AA

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Aphthae Management

• Acute, single episode• Severe: Prednisone 1mg/kg PO qam until pain resolves

• Topical clobetesol oint BID to ulcers

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Aphthae Management

• Recurrent• Workup

• HIV Ab

• CBC with diff, peripheral smear (heme/neutropenia)

• B12/folate/zinc/iron levels

• Inflammatory bowel disease

• Behcet’s disease

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Aphthae Management

• Recurrent• Treatment

• Colchicine 0.6mg PO BID-TID (SE: diarrhea)

• Dapsone

• Thalidomide

• Pentoxyfylline

• TNF inhibitors (adalimumab, etanercept, infliximab)

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A Note on Behçet’s Disease

• Multiorgan, inflammatory disease

• Old Silk Road (Turkish, Middle Eastern, Japan)

• VERY RARE

• 1990 ISG for Behçet’s Disease Criteria• At least 3 episodes oral aphthous ulcers in 1 year• Plus 2 of following

• Recurrent genital aphthae• Uveitis, hypopyion, or retinal vasculitis • Erythema nodosum or acneiform lesions • Positive pathergy test

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A Note on Behçet’s Disease• Multiorgan, inflammatory disease

• Old Silk Road (Turkish, Middle Eastern, Japan)

• VERY RARE

• 1990 ISG for Behçet’s Disease Criteria• At least 3 episodes oral aphthous ulcers in 1 year (1) Ask• Plus 2 of following

• Recurrent genital aphthae• Uveitis, hypopyion, or retinal vasculitis (2) Ophtho Exam• Erythema nodosum or acneiform lesions (3) Full Skin Exam• Positive pathergy test

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A Note on Behçet’s Disease

• Clinical concerns• Vascular

• Vascular aneurysms fatal

• Thrombophlebitis

• Arthritis

• Cardiac, GI, Renal, Neuro etc.

• Referral to Rheumatology

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Autoimmune Blistering Diseases

• Pemphigus vulgaris

• Bullous pemphigoid

• Cicatricial pemphigoid

• Linear IgA disease

• Bullous systemic lupus erythematosus

• Epidermolysis bullosa acquisita

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Pemphigus Vulgaris

• Auto-immune blistering disorder• Auto-antibodies to desmoglein 3

• Important to hold the epidermis together in skin and mucosa

• When severe can cause death

• Treatment• Prednisone

• Steroid-sparing immunosuppressants

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Pemphigus Vulgaris

• If persistent oral and genital ulcers• Consider this diagnosis• Consider other autoimmune bullous diseases

• Bullous pemphigoid• Cicatricial pemphigoid• Linear IgA disease• Bullous systemic lupus erythematosus• Epidermolysis bullosa acquisita

• Refer to dermatology for evaluation• Biopsy for H&E and Immunofluorescence

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