Iraqi Board Dermatology study materials
Iraqi Board Dermatology study resources

Iraqi Board Dermatology study plan

Iraqi Board Dermatology · Give each week a clear focus.

8 weeks · About 7 hours per week

Week 1

Basic sciences relevant to skin (structure, function, immunology, microbiology, genetics, pathology) & Diagnostic dermatology: history, morphology, dermatoscopy, and dermatopathology

  • Build a one-page schematic of epidermal turnover, barrier lipids, and dermal matrix composition, then label each layer's role in blister formation and wound healing from memory.

  • Map the inflammatory cascade of the skin (keratinocyte cytokines, Th1/Th17/Treg balance, mast cell and neutrophil recruitment) onto a diagram you can redraw in under five minutes.

  • Classify the primary and secondary lesions with precise definitions, and practise converting ten written morphological descriptions into a ranked differential diagnosis.

  • List the cardinal dermatoscopic structures (pigment network, globules, vessels, dots, regression) and match each to its histological correlate.

  • Explain the routine H&E report sequence (low power architecture, then cytology) and identify the four patterns of interface, spongiotic, psoriasiform, and lichenoid dermatitis by their key features.

Your checkpoint

A single annotated A4 'foundations sheet' (structure, immunology, morphology, dermatoscopy, histology patterns) plus 20 self-written morphology-to-differential drills with answers.

Week 2

Inflammatory and papulosquamous dermatoses (eczema, psoriasis, lichenoid and interface dermatoses) & Cutaneous infections and infestations (bacterial, viral, fungal, mycobacterial, parasitic, sexually transmitted)

  • Differentiate the clinical and histological features that separate psoriasis from nummular eczema, lichen simplex, and tinea corporis, and state the first-line treatment for each.

  • Construct a treatment ladder for atopic dermatitis by age and severity, including topical steroid potency selection, emollient strategy, and when to escalate to systemic or biologic therapy.

  • Distinguish lichen planus from lichenoid drug eruption and lupus interface dermatitis using distribution, mucosal involvement, and histology.

  • Organise cutaneous bacterial infections by organism and depth (impetigo, ecthyma, erysipelas, cellulitis, folliculitis, abscess) and match each to an appropriate antibiotic regimen.

  • Compare the viral exanthems and localized viral infections (herpes simplex, varicella-zoster, molluscum, HPV) by morphology, confirmatory test, and management.

Your checkpoint

A two-page comparison grid covering psoriasis versus eczema versus lichenoid dermatoses, plus a bacterial and viral infection 'organism-to-drug' table, each with at least 10 entries.

Week 3

Inflammatory and papulosquamous dermatoses (eczema, psoriasis, lichenoid and interface dermatoses) & Cutaneous infections and infestations (bacterial, viral, fungal, mycobacterial, parasitic, sexually transmitted)

  • Classify fungal infections (dermatophytes, Malassezia, Candida, deep mycoses) and select sampling method, KOH/culture interpretation, and therapy for each.

  • Outline the approach to cutaneous tuberculosis and leprosy, including the spectrum concepts, diagnostic tests available in Iraq, and multidrug regimens.

  • Describe scabies, pediculosis, and leishmaniasis: life cycle, diagnostic confirmation, and treatment including safety counselling.

  • Summarise sexually transmitted infections presenting with genital ulcers or discharge (syphilis, chancroid, herpes, gonorrhoea, chlamydia) with stage-appropriate serology and treatment.

  • Complete a self-quiz of 30 mixed inflammatory and infective vignettes and log every wrong answer with the corrected reasoning.

Your checkpoint

A completed error log of 30 vignette questions with corrected reasoning, plus a one-page 'genital ulcer differential' algorithm.

Week 4

Cutaneous tumors and lymphoproliferative disorders (benign, premalignant, malignant, melanoma) & Autoimmune, connective tissue, and blistering diseases

  • Build a melanoma recognition framework (ABCDE plus ugly-duckling and dermatoscopic algorithms) and apply it to 15 written lesion descriptions to produce a management decision for each.

  • Distinguish basal cell carcinoma subtypes, squamous cell carcinoma, and keratoacanthoma by clinical and histological features, and state margins and follow-up for each.

  • List the premalignant lesions (actinic keratosis, Bowen disease, leukoplakia, dysplastic naevus) with their transformation risk and treatment options.

  • Separate benign tumours and cysts (dermatofibroma, lipoma, epidermoid cyst, seborrhoeic keratosis, pyogenic granuloma) from mimics that require biopsy.

  • Contrast pemphigus vulgaris, bullous pemphigoid, dermatitis herpetiformis, and linear IgA disease by level of split, immunofluorescence pattern, and first-line therapy.

Your checkpoint

A tumour and blistering 'decision card' set: 12 lesion descriptions each resolved to diagnosis, biopsy decision, and treatment plan, with a separate immunofluorescence comparison table.

Week 5

Cutaneous tumors and lymphoproliferative disorders (benign, premalignant, malignant, melanoma) & Autoimmune, connective tissue, and blistering diseases

  • Outline the classification and work-up of cutaneous lymphoma, including mycosis fungoides staging and when to request clonal TCR gene rearrangement.

  • Explain connective tissue disease skin signs (lupus subtypes, dermatomyositis, systemic sclerosis, Sjogren) and the investigations that confirm each.

  • Interpret a written autoantibody and immunofluorescence panel and state the most likely diagnosis for each pattern.

  • Describe the urgent presentations of autoimmune blistering disease and the initial stabilization and referral steps.

  • Complete 25 mixed tumour and autoimmune vignettes, scoring above 70 percent before moving on.

Your checkpoint

A scored 25-question mixed assessment with a written review of every missed item, plus a one-page autoimmune bullous disease antibody table.

Week 6

Pigmentary, hair, nail, and mucosal disorders & Dermatologic surgery, lasers, and procedural dermatology

  • Differentiate vitiligo, post-inflammatory hypopigmentation, pityriasis alba, and indeterminate leprosy, and outline vitiligo treatment including phototherapy and surgical options.

  • Classify hair loss (androgenetic, alopecia areata, telogen effluvium, scarring alopecias) and select the appropriate test for each.

  • Recognise nail unit pathology: psoriasis, onychomycosis, melanoma, lichen planus, and paronychia, with sampling techniques.

  • Identify oral and genital mucosal disorders (oral lichen planus, leukoplakia, aphthosis, lichen sclerosus) and their malignant potential.

  • Describe the principles, indications, and complications of excisional and punch biopsy, cryotherapy, electrosurgery, and the main laser types.

Your checkpoint

A pigmentary-hair-nail-mucosa reference sheet plus a procedural 'indication to complication' table covering at least eight procedures.

Week 7

Pediatric dermatology and genodermatoses & Systemic disease and skin (internal medicine correlations, drug eruptions, cutaneous signs of systemic illness)

  • Summarise the neonatal and infantile dermatoses (seborrhoeic dermatitis, atopic dermatitis, haemangioma, milia, erythema toxicum) with expected course and when to intervene.

  • Recognise the major genodermatoses (neurofibromatosis, tuberous sclerosis, epidermolysis bullosa, ichthyoses, xeroderma pigmentosum) by their cutaneous markers and inheritance.

  • Identify cutaneous signs of systemic disease (acanthosis nigricans, erythema nodosum, pyoderma gangrenosum, dermatomyositis, paraneoplastic syndromes) and the internal work-up each triggers.

  • Classify drug eruptions by mechanism and morphology, and describe the emergency management of Stevens-Johnson syndrome and toxic epidermal necrolysis.

  • Apply a structured causality assessment to five written drug-eruption scenarios.

Your checkpoint

A paediatric and systemic-signs 'red flag' card set (at least 15 entries) plus five completed causality assessments.

Week 8

Dermatologic therapy: topical, systemic, biologic, phototherapy, and adverse effects & Research methodology, evidence appraisal, ethics, and patient safety

  • Compare topical vehicles and steroid potencies, and state the monitoring and adverse effects of systemic agents including methotrexate, ciclosporin, azathioprine, and isotretinoin.

  • Explain biologic selection and safety screening (tuberculosis, hepatitis, malignancy risk) and the monitoring schedule for each class.

  • Describe phototherapy modalities, dosing principles, and cumulative risk, and list the contraindications.

  • Appraise a study design (cohort versus case-control versus randomized trial), interpret sensitivity, specificity, and number needed to treat, and identify sources of bias.

  • Apply consent, confidentiality, and error-disclosure principles to written patient-safety scenarios.

Your checkpoint

A drug and phototherapy monitoring one-pager plus a completed 40-question timed mock exam with a written remediation plan for every domain scoring below 60 percent.

Milestones

Week 2: Recite the psoriasis-versus-eczema distinction and the first-line therapy for both without notes, and score at least 80 percent on a self-made 15-item morphology quiz.

Week 4: Correctly resolve at least 10 of 12 written tumour descriptions to diagnosis and management, and reproduce the immunofluorescence table for the four main blistering diseases from memory.

Week 6: Score at least 70 percent on the 25-item mixed tumour and autoimmune assessment from week 5, and name the test of choice for each of the four major alopecia categories.

Week 8: Complete the 40-question timed mock exam within the allotted time, with no domain below 60 percent and a written remediation plan for any that are.