Skin is part of the integumentary system and considered to be the largest organ of the human body. There are three main layers of skin: the epidermis, the dermis, and the hypodermis (subcutaneous fat). The focus of this topic is on the epidermal and dermal layers of skin. Skin appendages such as sweat glands, hair follicles, and sebaceous glands are reviewed in-depth elsewhere.
The first and outermost layer of skin is the epidermis. The epidermis is a stratified squamous epithelium that contains four to five layers depending on its location:
Deep to the epidermis lies the dermis. It is a thick layer of connective tissue consisting of collagen and elastin which allows for skin’s strength and flexibility, respectively. The dermis also contains nerve endings, blood vessels, and adnexal structures such as hair shafts, sweat glands, and sebaceous glands. The apical layer of dermis folds to form papillae that extend into the epidermis like tiny finger-like projections and is referred to as the papillary dermis, while the lower layer of the dermis is referred to as the reticular dermis.
The hypodermis is the third and deepest layer consisting mainly of adipose tissue.
There are four main functions of the skin: sensation, thermoregulation, protection, and metabolism 
After completion of a skin biopsy, the tissue is generally processed and sectioned for analysis with light microscopy. Skin tissue processing methods vary among laboratories; however, the paraffin technique is the most common. The standard steps for this process are fixation, dehydration, clearing, and paraffin infiltration. Fresh tissue is generally stored and transferred in 10% neutral buffered formalin fixative, which helps maintain tissue architecture by cross-linking lysine residues. Specimens get embedded in wax before mounting on glass slides for viewing. However, wax is not soluble in water or alcohol; therefore the specimens must undergo dehydration first. Alcohol dehydration is used to remove water from the sample. Alcohol is then removed by xylene as they are miscible in a process referred to as "clearing." The tissue is placed in a warm paraffin wax which replaces the spaces which water previously occupied. After the blocks have cooled, they are cut into thin slices, rehydrated with water, and then stained with stains such as hematoxylin and eosin. The amount of time for this process is dependent on tissue size, temperature, and reagents used.
Other techniques to make sections for light microscopy are frozen sections and semithin sections. Frozen sections are achieved by freezing tissue with liquid nitrogen and cutting it with a cold knife. This technique is faster than the paraffin technique. Semithin sections are used to see fine detail and are achieved by embedding sections in epoxy, allowing for thinner slices to be cut.
Specimens that require immunofluorescence undergo preservation in Michel's or Zeus solution rather than formalin.
Langerhans cell and melanocytes contain S-100. Immunofluorescence for antibodies against hemidesmosomes and desmosomes are commonly used to differentiate between blistering dermatoses like pemphigus vulgaris and bullous pemphigoid. Immunomapping may be helpful in distinguishing heritable blistering disorders.
Different layers of the epidermis are visible by examining sectioned epidermal tissue under hematoxylin and eosin staining under light microscopy:
The dermis is more visible with a Verhoeff’s stain. The interlacing collagen appears in red with elastic fibers in black. Blood vessels are surrounded by round, clear cells with well-defined borders named glomus cells.
Use of electron microscopy of skin, though limited, can be useful in identifying certain cell types such as Langerhans cells. These cells are characterized by Birbeck granules that appear as tennis rackets due to zipper like cross striations with a bulbous ending.
Melanocytes are neural crest-derived cells that sit in the stratum basalis of skin and hair follicles. These cells are responsible for the production of melanin from tyrosine. Melanin is a pigment that serves to protect DNA from UV radiation. Different skin tones are due to differences in the amount of melanin, size, and density once transferred from melanocytes to keratinocytes via melanosomes, rather than the number of melanocytes. Destruction and unregulated proliferation of melanocytes lead to various pathologies such as vitiligo and melanoma.
Langerhans cells are specialized dendritic cells found predominantly in the skin. Much like macrophages, these cells are derived from bone marrow monocytes and are capable of antigen presentation. Malignant proliferation of these cells are very rare and lead to a variety of diseases such grouped as Langerhans cell histiocytoses.
Parakeratosis refers to corneocytes in the stratum corneum with retained nuclei. Though normal is some parts of the skin, this is abnormal is most. Parakeratosis is a sign of increased cell turnover and can present in disorders such as psoriasis.
Hyperkeratosis refers to the thickening of the stratum corneum due to an abnormal increase in keratin. It is often present in a condition like eczema, warts, and corns.
There is a large amount of pathology associated with skin because of its vastness, diverse cell types, and constant proliferation.
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