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Facts about the skin from DermNet New Zealand Trust. Topic index: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z


Inflammatory skin diseases

Learning objectives
Introduction
Terminology in dermatopathology
Histopathology of common skin diseases
Potential errors in diagnosis
Activity

Learning objectives

Introduction

Pathological changes may arise in epidermis, dermis and/or subcutaneous tissue. The pattern of changes may allow a diagnosis to be made or it may be non-specific. The appearance of many skin diseases vary at different stages of their development and may be altered by attempted treatment and secondary changes such as scratching or infection.

Understanding the terminology used in describing pathological changes in the skin will help interpret pathology reports. The reporting pathologist will generally make or suggest a diagnosis or possible diagnoses, but it is especially important in inflammatory conditions that the report be correlated with the clinical features. If the clinical and pathological diagnoses do not tally, the case should be discussed with the pathologist to arrive at a consensus diagnosis (or to at least agree that a definite diagnosis is not possible at this stage).

The pathology of the following skin diseases will be outlined:

Terminology in dermatopathology

Descriptions refer to routine sections stained with haematoxylin and eosin (H&E).

Epidermal changes

Hyperplasia Increase in the number of cells
Hyperkeratosis Thickening of the stratum corneum
Orthokeratosis Hyperkeratosis without parakeratosis
Parakeratosis Flattened keratinocyte nuclei within the stratum corneum
Follicular plugging Hyperkeratosis within hair follicle
Hypergranulosis Thickened granular layer (may have associated hyperkeratosis)
Hypogranulosis Decreased thickness of granular layer (may have associated parakeratosis)
Acanthosis Thickened squamous cell layer
Psoriasiform hyperplasia Regular acanthosis, with elongation of rete ridges, as seen in chronic plaque psoriasis
Papillomatosis Elevation of adjacent dermal papillae above the surrounding epidermal surface
Pseudoepitheliomatous hyperplasia Extensive acanthosis simulating well-differentiated squamous cell carcinoma
Epidermal atrophy Decreased thickness of epidermis
Cellular vacuolisation Intracellular clear rounded spaces
Spongiosis Intercellular oedema between keratinocytes (sometimes associated with exocytosis)
Exocytosis Inflammatory cells within epidermis (usually refers to lymphocytes, and implies a benign process)
Acantholysis Separation & rounding up of keratinocytes because of loss of intercellular adhesions
Dyskeratosis Abnormally or prematurely keratinised eosinophilic keratinocytes, identified by prominent eosinophilic (red-staining) cytoplasm
Colloid bodies Non-nucleated eosinophilic deposits in lower epidermis or upper dermis formed from the intracellular filaments of dead keratinocytes, and may entrap immunoglobulin or fibrin
Corps ronds & grains Acantholytic dyskeratotic cells
Apoptosis ‘Programmed cell death’ of individual cells. Produces colloid bodies (which initially may contain shrunken dark nuclei).
Vacuolar degeneration Damage to the basal layer, with intracellular oedema and vacuoles. May be associated with colloid body formation and clear spaces at the dermal-epidermal junction, sometimes resulting in a subepidermal blister.
Spongiosis Spongiosis Parakeratosis Parakeratosis
Spongiosis Parakeratosis
Epidermal changes

Dermal changes

Melanin incontinence Melanin in the upper dermis following damage to basal cells
Dermal atrophy Decreased thickness of the dermis
Oedema Accumulation of interstitial fluid (may be difficult to identify and can have a similar appearance to mucin)
Hyalinisation Accumulation of dense ‘hard looking’ eosinophilic acellular material (stains red/pink)
Solar elastosis Accumulation of basophilic material (grey/blue) in the upper dermis of photo-aged skin
Sclerosis Hyalinised collagen with decreased fibroblasts
Mucin Pale blue threadlike or granular staining. Larger amounts ‘myxomatous’ (washed-out), resemble oedema
Calcification Dark blue brittle deposits: Metastatic – may involve blood vessels; Dystrophic – affects damaged tissue
Haemosiderin Brown iron-containing pigment from disintegrated red blood cells. Must be differentiated from melanin.
Cleft Empty space that previously contained material that has been dissolved in tissue processing such as fluid, crystals or lipid

Cells

Neutrophils Often referred to as ‘polymorphs’. Hypersegmented nuclei; cells clustered into abscesses or scattered in epidermis. In large numbers in the dermis in ‘neutrophilic’ dermatoses.
Eosinophils Segmented nuclei. Obvious numerous red (eosinophilic) granules in the cytoplasm. Associated with bullous disease, allergies, drug reactions and insect bites, but not specific. May be found in the epidermis or dermis.
Plasma cells Clock face nuclei, paranuclear clearing. Characteristic of chronic inflammation near mucous membranes and often seen around invasive tumours.
Lymphocytes & histiocytes The predominant cell type in most inflammatory skin diseases. Histiocytes are macrophages, and may be seen to have engulfed debris.
Multinucleated giant cells Large cells containing multiple nuclei, which are usually formed from histiocytes, but there are several different types, which may suggest particular infections or tumours.
Granulomas Nodular aggregate of histiocytes and other inflammatory cells. There are several subtypes, which may suggest specific infectious or non-infectious causes.
Red cells Extravasated into epidermis (rare) or dermis
Mast cells Classically have a ‘fried-egg’ appearance, but may be spindle or stellate shaped and very hard to identify without special stains.

Common patterns

There are two main schools of thought as to how inflammatory dermatoses should be described, but both are essentially a means to categorise changes into recognisable overall broad tissue reaction patterns, and then home in on more subtle changes to arrive at a diagnosis. One is based largely around the epidermal changes (spongiotic, lichenoid, psoriasiform or bullous), while the other identifies the basic pattern of inflammatory cell infiltration (superficial perivascular, superficial and deep perivascular, diffuse dermatitis, nodular dermatitis, and vesicular). Both systems have their merits, and many dermatopathologists use a combination of both.

Perivascular dermatitis Inflammatory cells are clustered around blood vessels. In superficial perivascular dermatitis the deeper dermal vessels are unaffected; in superficial and deep, all are affected.
Lichenoid dermatitis An infiltrate of lymphocytes affects and obscures the basal epidermis, classically with a band like pattern. Sometimes the infiltrate is patchy. There is associated basal cell degeneration.
Spongiotic dermatitis Typical of eczema, the epidermis shows patchy spongiosis, nearly always with associated exocytosis of lymphocytes.
Diffuse dermatitis A dense dermal infiltrate of mixed inflammatory cells which does not form obvious discrete nodules.
Nodular dermatitis Dense infiltrates of inflammatory cells in the dermis, often arranged in nodules.
Vesicular or bullous dermatitis A space is formed in the tissue (usually with fluid accumulation) to form a blister. Blisters are categorised by their location (intraepidermal,usually subcorneal or suprabasal, or sub-epidermal).
Normal-looking skin Clinical appearance or suspected diagnosis may guide pathologist to examine more carefully and to obtain special stains for surface fungi, mucin, mast cells etc.

Common skin diseases

Common skin diseases have characteristic microscopic appearances. A biopsy is often not necessary in typical cases because a diagnosis may be made clinically. In less typical cases, the pathology may be very helpful. However histological diagnosis is not always specific in these cases because the numerous inflammatory skin diseases have overlapping features, and the appearances may be markedly altered by attempts at treatment and the chronicity of the condition.

Eczema / dermatitis

A number of skin diseases are referred to as eczematous, in which there is diffuse ill-defined scaling and itching. Swelling and blistering may arise in acute eczema. Eczema or dermatitis are often synonymous. Link to a clinical description of dermatitis.

The histological features of eczema are:

Spongiosis Spongiosis Spongiosis Spongiosis
Eczema Spongiosis Inflammatory infiltrate
Histological features of eczema

Psoriasis

There are various subtypes of psoriasis, a common dermatosis with well demarcated erythematous scaly plaques. Link to a clinical description of psoriasis.

Due to the dynamic nature of psoriasis, this disease frequently does not show all classical histological features, but the typical changes of chronic plaque psoriasis are:

Parakeratosis Parakeratosis Parakeratosis Parakeratosis
Psoriasis Parakeratosis
Histological features of psoriasis

Lichen planus

Lichen planus is the idiopathic version of a group of lichenoid disorders characterised by scaling papules or plaques. Link to a clinical description of lichen planus.

The histological features of lichen planus are:

The majority of lymphocytes in the often dense infiltrate are memory cells, identified using histochemistry by positive CD8 and CD45 RO markers.

Direct immunofluorescence nearly always reveals fibrinogen within the colloid bodies. Occasionally IgM & complement are also detected. The immunofluorescence pattern is not diagnostic as the same reactants can also be seen in systemic lupus erythematosus and erythema multiforme.

Lichen planus Lichen planus Lichen planus Lichen planus
Lichenoid inflammation Immunofluorescence of lichen planus
Positive immunofluorescence – globular bodies and fibrinogen
Histological features of lichen planus

Bullous pemphigoid

Bullous pemphigoid is the most common subepidermal blistering disease. Link to a clinical description of bullous pemphigoid.

The histological features of bullous pemphigoid are:

Direct immunofluorescence reveals IgG and complement deposits in the basement membrane zone. (Biopsies for fluorescence should ideally be taken from erythematous but not yet bullous areas.) Indirect immunofluorescence will detect circulating antibodies. ELISA will be positive to 180 and 230kd BP antigens 2 and 1 respectively. Using skin separated by a salt splitting process, immunoreactants are seen to bind to the roof of the blister.

Bullous pemphigoid Bullous pemphigoid Bullous pemphigoid
Histological features of bullous pemphigoid

Vasculitis

Systemic vasculitis may affect the skin and vascular damage may be the main feature or a secondary feature in several skin diseases. Link to a clinical description of cutaneous vasculitis.

The histological features they have in common are:

Leucocytoclastic vasculitis Leucocytoclastic vasculitis
Histological features of leucocytoclastic vasculitis

Granuloma annulare

Granuloma annulare is the most common granulomatous disease of the skin. Its cause is unknown. Link to a clinical description of granuloma annulare.

The histological features of granuloma annulare are:

Acne

Acne is a special form of folliculitis. Link to a clinical description of acne.

The histological features of acne are:

Potential errors in diagnosis

General pathologists and experienced dermatopathologists report what they see. Their job is easier if a trained and experienced specialist dermatologist provides them with a good history and clinical differential diagnosis and carefully selected large skin biopsy. However many histology reports are from poor samples with inadequate clinical information.

Inflammatory dermatoses may be localised or generalised but a biopsy only provides the pathologist with a small sample, which may not be representative of the disease as a whole.

Activity

Find a dermatopathology report of an inflammatory skin disease. Rewrite the report in lay terms.

 

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Related information

References:

On DermNet NZ:

Information for patients

Other websites:

Books about skin diseases:

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Author: Clin Assoc Prof Amanda Oakley & Dr Paul Newman.

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If you have any concerns with your skin or its treatment, see a dermatologist for advice.