Connective Tissue Disorders (CTDs) | Medibuddy
2nd July 2023

Connective Tissue Disorders (CTDs)

CTDs are a heterogenous group of conditions that occur because of problems with collagen, and some have a vascular component as well. There are many CTDs, often similar in presentation, and can largely be split into inherited (such as Marfan’s syndrome and Ehlers-Danlos syndrome) and acquired CTDs (there are many, for which three are focused on below).

Cutaneous Lupus Erythematosus (CLE)

CLE is an uncommon group of skin disorders and occurs from autoimmune processes. It can be associated with systemic lupus erythematosus (SLE). There are many different types of CLE. Some of the key forms have been described below:

Acute CLE Presents as erythematous patches associated with a flare of acute SLE. These acute rashes include specific changes such as malar ‘butterfly’ rash presenting as redness and swelling over the cheeks and sparing the nasolabial folds and generalised acute CLE – a diffuse or papular erythema of the face, upper limbs, and trunk.
Subacute CLE Less commonly associated with SLE, with only approximately 50% having a mild form. The typical presentation is widespread, non-scarring round or psoriasis-like plaques. It usually presents in areas of sun exposure and can be triggered or aggravated by sun exposure.
Chronic CLE Discoid lupus is the most common form of chronic CLE, accounting for approximately 80% of cases and is much less commonly associated with SLE (1-2% of patients). Skin lesions are commonly on the scalp, ears, cheeks, nose, and lips. They are usually scaly plaques that heal slowly and can leave post-inflammatory pigmentation and scarring.
Chilblain lupus is a form of chronic CLE and causes cold-induced plaques on fingers and toes

A table summarising the key features in different forms of CLE.

Systemic Sclerosis

An autoimmune condition characterised by skin and internal organ fibrosis and vascular disease. There are two main subtypes according to the distribution of skin involvement: diffuse cutaneous systemic sclerosis (skin involvement across the whole body and early organ fibrosis) and limited cutaneous systemic sclerosis (skin involvement is limited to the face, hands, and feet).

The main skin manifestations are sclerodactyly, thickening and tightness of the skin of the fingers and toes, Raynaud’s phenomenon, telangiectasia on the face, chest and palms, and calcinosis on digits and extensor surfaces of arms. Patients will often exhibit microstomia, which can be defined as reduced interlabial distance of <4.5cm. In severe cases, patients can develop digital ulcers, which can result in dry gangrene and eventual loss of the tips of the fingertips.

Dermatomyositis

A rare multisystem disorder that can affect the skin as well as muscles and blood vessels. The exact underlying aetiology is not well understood. Triggers include medications, malignancy, viral infections, and certain trades, such as silica exposure. Additionally, most patients have disease-associated antibodies suggesting an autoimmune component, with ANA being the most common and anti-Mi-2 being the most specific. Skin manifestations can often have similarities with those seen in other CTDs, such as photosensitivity, calcinosis, and Raynaud’s phenomenon. More characteristic skin manifestations include Gottron’s papules and a heliotrope rash. The heliotrope rash presents on the face and upper eyelids as a bilateral lilac coloured discolouration. Gottron’s papules are characteristic purple papules and plaques that can be seen over the small joints of the hands.

Mobile app screenshots

Take your subscriptions with you

Our mobile app allows you to access your interview and exam question banks wherever you are.