Iraqi Board Dermatology study plan
Iraqi Board Dermatology · Give each week a clear focus.
8 weeks · About 7 hours per week
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.
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.
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.
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.
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.
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.
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.
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.