Showing posts with label Pachyonychia congenita. Show all posts
Showing posts with label Pachyonychia congenita. Show all posts

Thursday, August 3, 2023

Tutorial 15


Topics discussed in this Tutorial

Different types of Pustular Psoriasis

Amyloidosis

Juvenile Xanthogranuloma

Letterer Siwe Disease

Epidermolytic hyperkeratosis

Skin lesions in Thyroid disease

Variants of Discoid Lupus

Pigmented Purpuric Dermatoses

Pachyonychia Congenita

Leprosy


 What are the different types of pustular psoriasis?

Answer

There are the localised and generalised types. The localised include acral psoriasis or palmoplantar pustulosis. There is the Hallopeau variant. There is the juvenile napkin localised pustular psoriasis.
The generalised type includes the Von Zumbusch’s where there is a generalised sheet of pustules, the exanthematous where there are discrete pustular lesions. The Von Zumbusch’s like type may be due to steroid withdrawal.  Images in GSA of pustular psoriasis

Stable plaque psoriasis became pustular after intra articular steroid injection

What is the classification of amyloidosis?

Answer

There is a systemic and several localised variants. The systemic type of amyloidosis tends to localise to the fingers and face whereas the localised types particularly macular amyloid is on the upper back and lichen amyloid is primarily on the lower limbs as a brown papular scaly itchy rash.   Images in GSA        Note that amyloidosis can involve the larynx causing hoarseness and it is a cause of leonine facies.

Juvenile Xanthogranuloma   Image in GSA

These pinkish yellow nodules can occur at an early age. They may be single or multiple but are generally self-limiting. They particularly affect the eyes, the lungs, the liver and spleen. Note an association with neurofibromatosis and watch lymphomatoid papulosis as a differential diagnosis.


Periocular bleeding from capillaries in myeloma associated primary systemic amyloidosis.


Letterer-Siwe Disease

This is an acute histiocytosis usually present at birth presenting with seborrhoeic dermatitis papules and purpura. Often the condition occurs in crops. The purpura is particularly in the small of the back, the trunk and the axillae and babies with this condition may have recurrent infections. The Hand-Schuller-Christian type of histiocytosis occurs in two to five year olds. Occasionally in adults.   It will present with diabetes insipidus, proptosis and bone lesions. They may have chronic otitis media. Image in GSA

The eosinophilic granuloma variant tends to present with bone lesions and genital or perianal lesions.




What is epidermolytic hyperkeratosis?

Answer

This is mainly a histopathological finding with clumped keratohyalin granules and vacuolisation of the stratum spinosum and granulosum. It is a feature of several of the ichthyoses as well as the Vorner type of palmoplantar keratoderma. You can see it sometimes in epidermal nevi, in sporadic papules such as epidermolytic acanthomas and sometimes as a chance finding in normal skin. If you see it in an epidermal nevus the issue is often raised as to whether this is a form of mosaicism or whether bullous ichthyosiform erythroderma, which is a form of epidermolytic hyperkeratosis, may occur in a subsequent pregnancy.  Images in GSA of Epidermolytic hyperkeratosis




Skin Lesions and Hypo and Hyperthyroidism    

The skin is basically cold, dry and there are often dermatitic features particularly asteatotic eczema. There may be telangiectasia of the skin with mucin around the eyes causing swelling, pruritus is common, the fingers often have a doughy feeling and the patient may show carotenemia. The facial lines tend to be flattened because of facial oedema and the hair is often dry, coarse and thinned.

The skin lesions in hyperthyroidism include thyroid acropathy with drum like thickening of the nails and nail bed, the skin is often thin, sweaty, hyperaemic, the nails may show onycholysis and there may be pretibial myxedema.   



What are the major variants of discoid lupus?

Answer

They may be local or general. Lupus profundus occurs particularly on the lower legs. There may be no overlying features of lupus but just dermal atrophy or an area of fat atrophy. There is the angiolupoid variant, hypertrophic lupus erythematosus, and there is lupus pernio or chilblain lupus. These variants may represent about 6% of the total number of discoid lupus cases. Chilblain lupus can affect the nails with subungual hyperkeratoses and it can look red or there may be a bluish colouring of the nail plate and the nail can in fact crumble.

Dermnet on Cutaneous lupus


Tumid discoid lupus

Chilblain lupus of the toes




Pigmented Purpuric Dermatoses               

There are various names attached to this characteristic purpuric eruption on the lower legs and you will often call it a capillaritis because of the very small vessels that are damaged and the low level of that damage. Gravitational purpura is a common cause with associated varicose veins. However the named variants include lichen aureus, which is made up of orange/red macules that are grouped. They are sometimes solitary and there are only a few lesions. Image of lichen aureus

There is Schamberg’s variant, which gives a cayenne pepper type rash on the lower legs. Images in GSA

 The Gougerot-Bloom variant gives lichenoid like lesions, which are symmetrical on the lower legs  Image in GSA and there is the Majocchi variant that occurs in young adults sometimes with central clearing and an annular appearance . 

There is another variant called itchy purpura, which occurs in men on the lower legs with a progressive spread. It is useful to check for cryoglobulins, carbromal sensitivity and check for any abnormal immunoglobulins in the blood. There is also a rare contact purpura to some types of wool giving rise to pigmented purpuric dermatosis. I saw a case once in a foundry worker who wore a special woollen pair of trousers to protect himself from any direct heat damage. A similar rash on the lower legs can also be seen in golfers in the summer who walk the course.

Pigmented purpura or capillaritis




Pachyonychia Congenita

Patients with this condition show large thickened nails, leukoplakia, keratosis pilaris and often a pressure keratoderma on the feet. As an aside if you see grouped milia on the big toe think of dystrophic epidermolysis bullosa. Acral milia after blistering are also seen in PCT and EBA.

Thickened nails in pachyonychia congenita

Leprosy

In lepromatous leprosy you have symmetrical nodules, leg oedema, stuffy nose and the lesions have a diffuse edge. In borderline leprosy you have thickened nerves and in indeterminant leprosy you have macular lesions, pink in white individuals and white in black individuals. In borderline tuberculoid you have a diffuse outer edge but a defined inner edge, some sloping to the outer and lesions can be annular and band like. This is the commonest type of leprosy with anaesthesia, lack of hair and no sweating in the centre of the lesions. In tuberculoid leprosy it is often hyperpigmented with a sharp outer edge sloping to the centre. Note the difference with borderline. Again the lesions are anaesthetic with no hair and no sweating and there are thickened nerves particularly the ulnar and the posterior auricular. It is interesting though that if tuberculoid leprosy is on the face you do not get the lesional anaesthesia.

Images of Lepromatous leprosy in GSA

Images of Tuberculoid leprosy in GSA

Images of Indeterminate Leprosy in GSA



Tutorial 21

 Topics discussed in this Tutorial

Compare Alopecia areata, trichotillomania and traction alopecia

Cutaneous calcification

Pachyonychia congenita

Skin lesions in Hogkin's lymphoma

Eyelid papules

Genitocrural candidiasis

Clinical features of Lipoid proteinosis

Ichthyosis with mental retardation

Punctate keratodermas

Ichthyosis on the face

Compare alopecia areata, trichotillomania and traction alopecia.

Alopecia areata can occur in all age groups. There is a bald area with complete loss of hair follicles but preservation of the follicular openings.

In trichotillomania in adults it is usually occipital, in children it is temporal opposite to the handedness. Also adults tend to close crop the hair whereas in children it is left with very irregular lengths, which point irregularly in all directions.

In traction alopecia it usually is due to the hair being pulled up into a bun and it gives an ophiasis like pattern. If mainly affecting the frontal scalp it can look like frontal fibrosing alopecia. Other types of traction alopecia include marginal which is usually the forehead. Hot comb which involves the crown then spreads centrifugally (now called central centrifugal cicatricial alopecia) and the massage type alopecia.
Pressure alopecia occurs after surgery or in the neonatal period particularly on the occipital scalp.

The image below is of Trichotillomania



Cutaneous Calcification

This is usually considered under the headings of dystrophic, metabolic, idiopathic and normocalcemic. Dystrophic is just localised injury due to trauma or inflammation. It can occur in degenerative processes such as pseudoxanthoma elasticum and also in benign and malignant neoplasms.

Metabolic calcification is found with hyperparathyroidism and sarcoidosis, vitamin D intoxication, the milk alkali syndrome or in destructive bone disease seen in myeloma and Paget’s disease of bone.

Idiopathic calcification can be due to calcinosis universalis, which is a primary disorder seen in girls and young children where sinuses may develop. Other forms are cutaneous calculus, pinnal calcification and tumoral calcinosis. Universal calcification can be a secondary feature of dermatomyositis, scleroderma, lupus and acrodermatitis chronica atrophicans.

Normocalcemic cutaneous calcification is seen in chronic renal failure and pseudo hyperparathyroidism.

Pineal calcification occurs in Addison’s disease, ochronosis, acromegaly, dermatomyositis, hyperthyroidism, systemic chondromalacia and familial cold hypersensitivity.

Hypocalcemic calcification causes dry skin, alopecia, brittle nails that are grooved. You may have chronic mucocutaneous candidiasis.

Intravenous Bleomycin and calcium gluconate injections can give localised calcification.

The image below is of Calcification in Scleroderma




Pachyonychia Congenita

This can look like large corns on weight bearing areas with the plantar keratoderma.

Adolescent striae obviously presents in adolescents. The site of choice is usually the lumbo sacral area in boys whereas in girls it is the breasts and hips.

Question

What are the skin lesions of Hodgkin’s disease?

Answer

They are often non-specific in 30% to 50% of cases and include pruritus, prurigo, herpes zoster, addisonian pigmentation particularly in the axillae, groins and nipples.

The image below is of Pachyonychia Congenita



Causes of Eyelid Papules

They include acnitis, syringomas, molluscum, amyloid, lipoid proteinosis, sarcoidosis, rosacea, Fabry’s disease and trichoepitheliomas. Most trichoepitheliomas are skin coloured or yellow or pink. They can occasionally be bluish because of pigment. The inheritance is probably autosomal dominant but there are more females than males.


The image below is of Syringomas



What are the types of genitocrural candidiasis?

Answer

Firstly there is the intertrigo like, then there is a pustular type, and also an erosive type on the scrotum. There is an ulcerating type and there is a balanitis type on the penis. Around the perianal and natal cleft candida looks like psoriasis and there is the rare granulomatous type of candidiasis seen in neonates.


The image below is of groin candidiasis.



What are the clinical features of lipoid proteinosis?

Answer

Hoarseness with thickening and stiffening of the tongue, eyelid papules and papules on the hands. The nodular lesions on the elbows look like xanthomata.

The image below is of eyelid papules in lipoid proteinosis.







Adolescent striae obviously presents in adolescents. The site of choice is usually the lumbo sacral area in boys whereas in girls it is the breasts and hips.
What are the other causes of striae?

Answer

Pregnancy, drugs, collagen diseases and Cushing’s disease. Note that there are no striae with Ehler’s Danlos patients when they are pregnant.   You can get a rare horizontal striae on the nose in children under 10 with a defined ridge on the bridge of the nose, which is related to the growth of underlying structures. It just disappears.


The image below is of steroid induced striae.





What are the causes of ichthyosis with mental retardation?

Answer

X-linked ichthyosis sometimes, Sjogren Larsen, Rudd’s syndrome, Richner Hanhart syndrome and Downs syndrome.

The image below is X linked ichthyosis




What are the causes of punctate keratoderma?

Answer

In an infant it is the Richner Hanhart syndrome. In an adolescent it is disseminated punctate keratoderma and Darier’s disease is usually seen in adults though it is variable.



Ichthyosis on the Face

In ichthyosis vulgaris the face involvement includes the forehead, cheeks and scalp. In X-linked ichthyosis it tends to involve the periphery of the face.


The image below is of X linked ichthyosis.