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Dermatology Series: Hair Loss

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Summary

The course "Dermatology in Primary Care: Hair Loss", led by Dr. Rajani Tripathi, a specialist in dermatology, and scheduled for 15 Oct 2024, offers an in-depth examination of hair loss causes, types, diagnosis, and treatments. Providing invaluable information on the hair growth cycle and the classification of alopecia, this session also delves into specific conditions like Telogen Effluvium, Anagen Effluvium, and Alopecia Areata. Participants will also understand the related issues such as Madarosis and Androgenic Alopecia (Male Pattern Baldness). This session is beneficial for medical professionals aiming to improve their understanding and patient care when dealing with hair loss issues.

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About the MedAll Primary Care CPD Programme

We are passionate about making great medical education easily accessible and we power thousands of medical courses and events every year. In light of the increasing commitments faced by healthcare professionals, including the rising cost of living and strained practice finances, we felt compelled to do something. It's why we have introduced a flexible, easy access CPD programme for doctors, nurses and other healthcare professionals working in primary care. We recognise that the high expense of traditional CPD update courses is a significant barrier, and by collaborating as an entire primary care community we hope we can offer a practical, accessible alternative that delivers exceptional value.

About our speaker: Dr. Rajani Tripathi

Dr. Rajani Tripathi is a General Practitioner (GP) at Modality - Handsworth Wood Medical Centre in Birmingham.

Who Should Join?

✅ GPs

✅ GP Trainees

✅ Primary care and practice nurses

✅ Practice pharmacists

✅ Other allied healthcare professionals in Primary Care

Accreditation Note

This event is not formally accredited by an external organisation for CPD points. The current guidance for GP CPD is that it is appropriate that the credits you self-allocate should equal however many hours you spent on learning activities, as long as they are demonstrated by a reflective note on lessons learned and any changes made or planned (if applicable).

Learning objectives

  1. Define and differentiate the types of alopecia, including non-scarring and scarring alopecia.

  2. Identify the typical growth and resting phases of the hair growth cycle and how these phases are impacted in various forms of alopecia.

  3. Diagnose hair loss conditions based on signs, symptoms, and patient medical history, with a focus on conditions like Telogen Effluvium, Anagen Effluvium, and Alopecia Areata.

  4. Understand the role of lab and skin investigations in diagnosing alopecia and interpret common test results related to hair loss conditions.

  5. Effectively manage and treat hair loss conditions in primary care, with knowledge of both medical and non-medical treatment strategies.

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Computer generated transcript

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The following transcript was generated automatically from the content and has not been checked or corrected manually.

Dermatology in Primary Care: Hair Loss Dr Rajani Tripathi, GPSI in Dermatology MBBS, MD (Family Medicine, USA) MRCGP 2018, DPD (distinction) 15 Oct 2024 Hair loss Non scarring alopecia Scarring alopecia Ref: Habif Hair growth cycle  Anagen phase –growth phase 90-95% of hair is in this phase. Its duration determines the length of hair, and for scalp hair, it is 2-6 years  Catagen phase - involution phase < 1% of scalp hair is in this transitional phase. Acute follicular regression occurs.  Telogen phase- resting phase 5-10% of scalp hair in this resting phase. It lasts for 2-3 months; club hair is ejected and replaced by new anagen hair. Ref: Habif Ref: Rooks 25-100 telogen hair is shed dailyClassification of alopecia Focal or diffuse and the presence and absence of scarring (Habif, 2010).  Diffuse, non-scarring, e.g. Telogen effluvium, anagen effluvium, diffuse alopecia areata, male and female pattern baldness, alopecia associated with systemic disease, e.g. thyroid, iron deficiency, SLE.  Focal, non-scarring, e.g. localized alopecia areata, traction alopecia, trichotillomania, Syphilis, Tinea capitis.  Focal, scarring e.g. lichen planopilaris, frontal fibrosing alopecia, acne keloidalis, folliculitis decalvans, dissecting cellulitisTypes of alopecia SCARRING ALOPECIA NON-SCARING ALOPECIA  Hair follicle is permanently damaged and  Hair follicle is not damaged, hair growth replaced by scar tissue cycle is affected e.g increased shedding or slowed/reduced growth of new anagen  Hair regrowth will not occur. hair.  E.g Lichen planopilaris, frontal fibrosing  Hair is likely to grow. alopecia, folliculitis decalvans, acne keloidalis, Kerion  E.g alopecia areata, androgenetic alopecia, Telogen effluvium, anagen effluvium, trichotillomania T elogen Effluvium  Diffuse hair loss, body hair may be involved  About 70% of anagen hair prematurely enters telogen reversing the usual ratio  Noticed 3-6 months after the triggering event  New hair growth pushes out telogen hair and increases hair fall  Fine new hairs can be seen.  Usually acute and lasts about 6 months but may be chronic  More common in women, e.g. postpartum.  Affects any age group and both sexes Ref: Dermnet Common causes ACUTE CHRONIC  Stress  Iron deficiency  Acute illness- pyrexia  Thyroid disorder  Postpartum, stopping contraceptive pills  Chronic inflammatory conditions-  Major injury, Recent surgery malabsorption, hepatic, renal disorders,  Crash diet, weight loss SLE  Jet lag  Drug induced-Acitretin  Zinc deficiency  Excessive sun exposure No trigger is identified in 1/3 of the cases Arrest of hair growth is often mirrored in nails by Beau line.  Beau’s line can help estimate timing as fingernails grow out in 5 months.  Telogen effluvium does not cause complete baldness but may unmask male or female pattern baldness Ref: Dermnet Investigation  FBC, Ferritin (aim over 70)  TFT  U&E  LFT  Zinc levels  Vitamin D  Other test depends on history and examination: ANA for suspected lupus, syphilis serology Dermoscopy: thinning of hair but scalp otherwise normal  Skin biopsy is rarely needed.  Treatment  Gentle handling of hair  Nutritious diet with plenty of protein, fruit and vegetables  Treat the underlying cause.  Psychoogical effects of hair loss can be huge  Unless the trigger is repeated, there will be spontaneous complete regrowth within 3-6 months Anagen effulvium  Abrupt hair shedding during the anagen (growth) phase  Caused by acute injury to the hair follicles due to :  Infection- boils, abscess, Tinea capitis  Drugs  Chemotherapy- recovers fully within 3-6 months  Radiation- regrowth may be incomplete or may not occur  Autoimmune – AA, alopecia totalis, alopecia universalis, pemphigus vulgaris Alopecia areata • Autoimmune condition affecting hair follicles • T-cell mediated • Associated with – stress, atopic dermatitis • Genetic predisposition • Can occur at any age peak 2nd -4th decade • Equal in male and female • Circumscribed smooth bald patch. • Scalp, beard, eyebrows, eyelashes, axillary and pubic hair affected Ref: PCDS Three stages:  1) Sudden hair loss  2) Enlargement of bald patch/patches  3) Hair regrowth • Relapse and remittance• Dermoscopy: Exclamation mark hair is seen in the periphery of the lesion during the active phase. • Black dots and broken hairs are also seen • Yellow dots and short vellus hair signify non-active disease. Ref: Dermatoscopedia• Patches may coalesce or progress to complete loss of scalp hair (Alopecia totalis) or total body hair (Alopecia Universalis).  Ophiasis- Occipital and lateral scalp affected, bald patch may encircle the scalp • Sisaipho- hair loss in the frontal, temporal and parietal scalp • The initial hair that grows is usually fine and non-pigmented, Ref: Dermnet then gradually regains its normal colour and calibre • Patients with a mixture of grey and pigmented hair, it prefers pigmented hair. ‘sparing phenomenon’ • Moth- eaten Alopecia is a feature of secondary Syphilis Ref: PCDS Nail changes like pitting, hammered brass appearance, ridging, trachyonychia, and red spots on the lunula are present in severe disease.  Treatment:  Spontaneous recovery  Very potent topical steroids like clobetasol cream or scalp application for 3/12.  Intralesional corticosteroids like Triamcinolone. Stronger evidence that topical  Contact sensitizers like DCP (Diphenylcyclopropenone)  NICE recommends a JAK inhibitor like Ritlecitinib in patients 12 years of age and older, but this recommendation has not yet been translated into practice.  Others: PRP, Wigs Ref: Rooks Poor prognostic factors  Childhood onset  Severe hair loss  Ophiasis  Bald patch lasting more than a year  Nail disease  Family history of AA  Coexistent autoimmune diseases Madarosis Loss of eyelashes or eyebrows.  Causes 1. Alopecia areata 2. Hypo/ hyperthyroidism 3. Iron deficiency 4. Eczema, Psoriasis 5. Infection: Staph, Herpes simplex, Syphilis, Leprosy 6. Treatment-induced : chemo, radiotherapy, laser treatment 7. Trichotillomania 8. Causes of scarring alopeciaAndrogenic alopecia- Male pattern baldness  Diffuse hair thinning and balding in adult male.  Cause- a combination of hormones and genetic predisposition  Sensitivity to the effect of DHT in some areas of the scalp.  DHT reduces the anagen phase to weeks or months  DHT production is regulated by 5-alpha reductase enzyme.  Affects 50% male Caucasian by age 50 and 80% by age 70  Chinese and Japanese men are less affected  Usual onset is mid to late 30s Ref : PCDS Progressive fronto-temporal hair recession and thinning over the crown, vertex.  Miniaturization of hair follicles occurs and progressively fewer and finer hair  No inflammation, no scarring Ref: Dermatoscopedia Treatment  Not available in NHS  Topical Minoxidil 5% (OTC) BD only works in 40 % of patients.  Response to treatment is assessed in 6 months and needs to be used long-term to prevent relapse.  Minoxidil is best used in early-stage  Private treatment options- Finasteride 1mg OD, Dutasteride, oral Minoxidil, PRP, Hair transplant Female pattern baldness  Genetic predisposition, genes inherited from either parent.  Unclear if androgens play a role, mostly normal  Women with hyperandrogenism e.g. PCOS, are affected  Role of estrogen is uncertain, but common after menopause  Can affect women at any age  Presentation: increased hair shedding  Frontal hairline margin is usually preserved with thinning over the middle part, progressing from vertex to frontal scalp Ref: PCDS Treatment  Not available in NHS  Topical Minoxidil 2%, 5% OD - OTC  Block effect of androgens: Spironolactone, cyproterone, finasteride  Low-dose oral minoxidil (0.625mg OD)  Hair bulking fibre powder, wigs, hair transplantation  PRP Traction Alopecia  Hair loss caused by prolonged and repetitive tension on scalp hair, e.g. tight corn rows, ponytails, weaves, braids, hair extensions, hot irons, and tight hair rollers.  Can also be due to the weight of excessively long hair.  Incidence increases with age due to prolonged history of the hair care routine  Hair loss occurs at the site of maximum traction, commonly along the hair margins – “marginal alopecia”  Fringe sign- retention of hair in frontotemporal margin Ref: Rooks Can present with itching, redness, scaling, folliculitis, broken hairs and thinning.  It is differentiated from alopecia areata by the lack of exclamation mark hairs.  Initially, it is non-scarring, but prolonged excessive tension leads to the destruction of hair follicles Treatment: Ref: Dermnet  Avoid high-tension hairstyles and treatments.  Cut long hair  Avoid heat and chemical Trichotillomania • Irresistible urge to pull own hair • Affects 4% of general population • More common in children, peak in pre- school years and early adolescence. M=F • As age increases, it is seen more in females. • Cause: possible genetic tendency • Psychological associations include anxiety, obsessive-compulsive disorder, and depression. • Can be a coping mechanism for anxiety and is commonly associated with other habits like nail biting, nail/skin picking, lip biting, etc.• The behaviour is often ritualized to a similar place, time of day, or situation, e.g. reading, watching TV, or talking on the phone. • There may be a compulsive urge that is relieved by the act of hair-pulling. • Pleasurable and not described as painful • Hair loss is seen in the scalp, eyebrows, eyelashes, and pubic hair. • Hairs of varying lengths giving ‘ wire brush appearance, and normal-appearing areas. • Split hair, broken hair, newly growing hair with tapered ends • Normal underlying scalp, but scratches, and erythema from pulling may be seen • Areas that are accessible to the dominant hand• If hair is repeatedly pulled out, damage to the hair follicles can cause irreversible scarring, folliculitis even keloid • Rare complication: trichobezoar and the Rapunzel syndrome with gastrointestinal obstruction. • Mx- Education of parents/caregivers. -Behavior modification, habit reversal - reducing stressors -TCS, SSRI. Usually benign and self-limiting in children. In adolescents and adults, it is episodic and chronic and associated with more psychopathology Ref: Dermoscopedia Frontal fibrosing alopecia  Scarring alopecia in which there is recession of the frontal hairline.  Typically seen in postmenopausal women. Younger men, women, and children of all ethnic groups can be affected.  Genetic, hormonal, autoimmune, inflammatory and environmental factors have been suggested.  Seen in patients with hypothyroidism, autoimmune diseases like lupus and RA and regular sunscreen use!  Contact allergy to fragrances, cosmetics, moisturising cream, suncream Ref: PCDS suggested but unconfirmed Linear band of hair loss and sideburns are also lost. Symmetric.  There may be a recession of the posterior hairline also.  Loss of vellus hair  Skin in the affected area is pale, and shiny and does not show sun damage seen in the forehead  Perifollicular erythema and hyperkeratosis at the hairline.  Papules may be seen on the cheeks due to the involvement of vellus hairs  Hair loss can affect all parts of the body. Eyebrows may be affected before scalp  Itch and pain are common early symptoms, and sometimes may have a facial rash- skin-coloured or yellowish follicular papules Ref: Dermnet• Dermoscopy: absent follicles, tubular perifollicular scale, perifollicular erythema. Perifollicular pigmentation. ‘Lonely hair’ in the bald area. • Diagnosis: skin biopsy to rule out other causes of scarring alopecia • Treatment: • Topical steroids like betacap scalp application • Anti-inflammatory antibiotics like Tetracyclines. REF: Starace M, Orlando G, Iorizzo M, Alessandrini A, Bruni F, • Hydroxychloroquine S, Lobato-Berezo A, Mernissi FZ, Paoli J, Patrí A, Sabban ENC, Sławińska M, Sobjanek M, Zaar O, Pellacani G, Piraccini BM. • Rituximab, Adalimumab Clinical and Dermoscopic Approaches to Diagnosis of Frontal • Hair transplant once the disease activity has settled International Dermoscopy Society. Dermatol Pract Concept. 2022 Jan 1;12(1):e2022080. doi: 10.5826/dpc.1201a80. PMID: 35223189; PMCID: PMC8824238. • Prognosis- slowly progressive, self-limiting, burns out after several years Lichen planopilaris • Lichen planus of hair follicles • Scarring hair loss • Mostly affects young adult women F:M::8:1 • Cause- autoimmune and rarely genetic or drug-induced. • Patch commonly in vertex and patches can merge • Associated redness, itching, pain, perifollicular scales Ref: Habif • Shiny waxy scalp • Can affect scalp, eyelashes, eyebrows, axillae • Dermoscopy: tubular perifollicular scaling. Erythema, white dots. • Skin biopsy- lymphocytic folliculitis • Treatment aim is symptom control and slow progression • Potent topical steroid, high dose Lymecycline 408 mg BD or Doxy 100 mg BD. • Hydroxychloroquine • Other; Acitretin, Ciclosporin, Methotrexate • Prognosis unpredictable- may burn out or be progressive Ref: PCDSCentral centrifugal cicatricial alopecia (CCCA)  Scarring alopecia  Most common form seen in Afro-Caribbean women, may be seen in men  Middle-aged women are most affected  Cause- unknown, multifactorial- genetic autoimmune, fungal/bacterial infection  Hair loss in the crown and extends in a centrifugal manner, incomplete alopecia as some hair remains  Hair breakage is an early sign Ref: Dermnet Scalp may appear shiny  Tenderness, itching and burning is common  Diagnosis- clinical feature + scalp biopsy from active edge  Treatment goal is to stop the progression  Dermovate or intralesional steroids  Tacrolimus  Tetracyclines- Doxycycline, Lymecycline if pustules present  Hydroxychloroquine, ciclosporin  Avoid hairstyles causing discomfort and scalp irritation Folliculitis DeCalvans  Chronic neutrophilic inflammation causes scarring hair loss th th  4 -5 decade, Male predominance  Cause: Abnormal immune response to Staph aureus  Affects scalp around crown, may affect beard, axillae, limbs, pubic hair  Irregular scarring and hair loss, scalp induration  Follicular pustules and crusts Ref: Dermnet  Tufting giving a ‘doll’s hair’ appearance  Itch, discomfort, pain Diagnosis- swab for microbiology and Mycology  Skin biopsy- neutrophilic infiltrate  Treatment: -Antibiotics- oral tetracyclines, azithromycin, Rifampicin and Clindamycin -Others: Isotretinoin, TNFi, IVIG -Photodynamic therapy  Fluctuating exacerbation and remission over many years.  Treatment reduces inflammation in the short term, but unclear if it affects long term prognosisAcne Keloidalis nuchae/folliculitis keloidalis  Chronic inflammation of the hair follicles of the neck leading to hypertrophic scarring.  Most prevalent in Afro-Caribbean males with curly hair.  M:F::20:1 Causes  Injury during close shaving of hair  Ingrown hair irritating the hair follicles Ref: Dermnet  Irritation from shirt collar  Chronic low-grade bacterial infection Itchy round small papules at the back of the neck  Scratching can lead to secondary bacterial infection and develop pustules  Leads to scarring, and scars can develop into keloid-like hairless areas.  Diagnosis is clinical  Biopsy if diagnostic uncertainty.  Biopsy will show neutrophilic inflammationTreatment- is difficult GENERAL MEASURES SPECIFIC MEASURES  Ensure the helmets and collars do not  Topical steroids like Dermovate, intralesional steroid  Antibiotics-Tetracycline or Doxycycline for 3 rub the back of the neck. months  Avoid shaving hair  For more severe cases Clindamycin300 mg BD +Rifampicin 300 mg BD for 3-6 months  Stop grease and pomades  Oral Isotretinoin,  Laser ablation  Antimicrobial cleansers like Dermol or Hibiscrub Pseudopelade of Broq  Unusual form of permanent hair loss of unknown cause.  Caused by atrophy of hair follicles rather than scarring.  Affects middle-aged and older women commonly  Affects vertex, parietal scalp and rarely beard  Single or multiple smooth patches, may merge  Patches described as ‘footprint in snow’ Ref: Dermnet  No scales, skin normal colour. Perifollicular redness in early stage.  Hair may be easily pulled from the edges if active Diagnosis reached by excluding other scarring alopecia  Scalp biopsy shows thin epidermis, sclerotic dermis and fibrotic streamers down to the fat layer.  No inflammation is seen in the biopsy.  No known treatment to stop the process or regain hair.  Usually, it is a slow process with a small area of hair loss.Dissecting cellulitis/Perifolliculitis capitis abscedens et suffodiens  Uncommon cause of scaring alopecia.  Most common in Afro-Caribbean men in their 30s-50s  Cause: A defect in follicular keratinisation causes occlusion and Ref: Dermnet inflammatory destruction of the follicle.  It mainly affects the vertex and posterior scalp.  Follicular and perifollicular pustules, nodules, pseudocysts with purulent exudate and pain  Interconnecting sinuses  Hair loss and keloid Patients may have follicular occlusion syndrome- HS, nodulocystic acne and pilonidal disease  Dx: clinical  Treatment: - Antibiotics- Tetracyclines, Erythromycin - Isotretinoin - Oral/intralesional corticosteroids - Analgesia, topical antiseptic - Others: TNFi, Laser , Surgical Tinea capitis/ Kerion  Fungal infection of the scalp involving skin and hair  Trichophyton tonsurans and Microsporum canis (pets) predominate  Affects preadolescent children, seen in siblings, peak age 3-7 years Ref: PCDS  Also affects immunocompromised adults  Risk factors: animal contact, household crowding, warm humid environment Ref: Dermnet Single or multiple patches  Hair loss, broken, black dots ringworm  Scaling, w/ or w/o hair loss  Yellow crusting and matted hair. Ref: Habif, 2010  Itching maybe present  Cervical lymphadenopathy  Kerion- boggy mass of inflammatory tissue with pustules. Dermoscopy: scale, broken hair, loss of pigment. Comma hair, corkscrew hair  Skin scraping and plucked hair follicle for mycology  Risk of scarring alopecia, start treatment  Contagious- sharing hairbrush, pillow, hat, helmet, towel Ref: Dermnet Treatment  Terbinafine for 4 weeks, first choice weight > 40 kg =250 mg OD weight 20-40 kg = 125 mg OD weight up to 20 kg = 62.5 mg OD (Ref: PCDS)  Itraconazole is an alternative for adults  Griseofulvin in children 6-8 weeks, more effective against M. canis  Griseofulvin is the only licensed oral antifungal agent for the treatment of fungal scalp infection in children in the UK (Ref: NICE CKS)  Itraconazole is not licensed for the treatment of fungal scalp infection in the UK(Ref: NICE CKS). Kerion: Terbinafine for 12-16 weeks  Treat patient and family members with Ketoconazole shampoo 2x week for 2 weeks. Reduces infectivity and shedding of spores  Pet should be examined by Vet and treated if indicated . Ref: PCDS Charities and support group  Alopecia UK; Alopecia UK  British Association of Dermatologists (bad.org.uk) for PILs