Cryotherapy, also known as cryosurgery, is a commonly used in-office procedure for the treatment of a variety of benign and malignant lesions. In one report, cryotherapy was the second most common in-office procedure after skin excision. The mechanism of destruction in cryotherapy is necrosis, which results from the freezing and thawing of cells. Treated areas reepithelialize. Adverse effects of cryotherapy are usually minor and short-lived.
Dermatologists have used cryotherapy since the turn of the century. After the development of the vacuum flask to store subzero liquid elements, such as nitrogen, oxygen, and hydrogen, the use of cryotherapy dramatically increased. By the 1940s, liquid nitrogen became more readily available, and the most common method of application was by means of a cotton applicator. In 1961, Cooper and Lee  introduced a closed-system apparatus to spray liquid nitrogen. In the late 1960s, metal probes became available. By 1990, 87% of dermatologists used cryotherapy in their practice.  The general advantages of cryotherapy are its ease of use, its low cost, and its good cosmetic results. Most skin cancers are treated with excision or other destructive procedures, such as electrodesiccation and curettage. Superficial basal cell skin cancers  and Bowen disease can be treated with cryotherapy.
Recurrence rates for primary basal cell carcinoma vary with treatment modality. The 5-year recurrence rate for cryotherapy may be as low as 7.5% if lesions are chosen judiciously.  This percentage compares favorably with published recurrence rates following other procedures. Published rates include surgical excision, 10.1%; curettage and electrodesiccation, 7.7%; radiation therapy, 8.7%; and all non-Mohs modalities, 8.7%. Because these percentages are derived from various studies, rather than one randomized controlled study comparing the different modalities, they should be viewed as rough approximations. Well-circumscribed tumors are most suitable for cryotherapy. The indolent local growth of these well-circumscribed tumors accounts for the high cure rates quoted in the literature.
In most instances, reimbursement for cryotherapy treatment of skin cancers is at the same rate as for destruction of benign lesions.
Mechanism of Action
The mechanism of action in cryotherapy can be divided into 3 phases: (1) heat transfer, (2) cell injury, and (3) inflammation.
The mechanism by which cryotherapy destroys the targeted cells is the quick transfer of heat from the skin to a heat sink. The most commonly used cryogen is liquid nitrogen, which has a boiling point of -196°C. The rate of heat transfer is dependent on the temperature difference between the skin and the liquid nitrogen.
When using the spray cryotherapy technique, the liquid nitrogen is applied directly on the skin, and evaporation (boiling heat transfer) occurs in which the heat in the skin is quickly transferred to the liquid nitrogen. This process results in the liquid nitrogen evaporating (boiling) almost immediately.
When using a cryoprobe for cryotherapy, conduction heat transfer occurs where the heat is transferred via the copper-metal probe.
Cell injury occurs during the thaw, after the cell is frozen. Because of the hyperosmotic intracellular conditions, ice crystals do not form until -5°C to -10°C. The transformation of water to ice concentrates the extracellular solutes and results in an osmotic gradient across the cell membrane, causing further damage. Rapid freezing and slow thaw maximize tissue damage to epithelial cells and is most suitable for the treatment of malignancies. Fibroblasts produce less collagen after a rapid thaw. Therefore, a rapid thaw may be more suitable for the treatment of keloids or benign lesions in areas prone to scarring. 
Freeze damage can be seen when a steak is defrosted from the freezer. The steak juices that are seen when fully thawed represent the intracellular liquid that has escaped because of the damage to the cell wall. Low temperature also ensures maximum damage by further concentrating electrolytes intracellularly.
Keratinocytes need to be frozen to -50°C for optimum destruction. Melanocytes are more delicate and only require a temperature of -5°C for destruction. This fact is the reason for the resulting hypopigmentation following cryotherapy on darker-skinned individuals. Malignant skin cancers usually need a temperature of -50°C, while benign lesions only require a temperature of -20°C to -25°C.
The last response to cryotherapy is inflammation, which is usually observed as erythema and edema. Inflammation is the response to cell death and helps in local cell destruction.
Various lesions have been treated with liquid nitrogen. Because of the histologic differences in lesions, different freeze-thaw cycles are used to successfully destroy them. For most of these lesions, cryotherapy is not the only and often not the best modality for treatment. However, it does represent a valuable alternative for selected patients. For some lesions, such as actinic keratoses, warts, and seborrheic keratoses, cryotherapy is the standard first-line therapy. The time estimates given below must be adjusted depending on the skin temperature, local circulation, skin pigment, and method of delivery. Overfreezing can produce permanent hypopigmentation and scarring.
For melasma, a light, uniform freeze with feathering completed every 4-6 weeks can produce a good cosmetic result in some patients. Other modalities, such as topical depigmenting agents, sunscreens, and chemical peels, are more commonly used to treat melasma.
For tattoos, two 30-second freeze-thaw cycles with 1-mm margins performed every 4-6 weeks can improve some lesions. Newer modalities, especially laser therapy, are more suitable for most tattoos.
Idiopathic guttate hypomelanosis can be treated with one 5-second freeze with feathering performed every 4-6 weeks.
Lentigo can be treated with one 5- to 10-second freeze with feathering completed every 4-6 weeks until resolved. Often, one treatment is all that is required.
Cryotherapy for melanocytic nevi generally is not recommended because these lesions should undergo histologic evaluation. Furthermore, atypical histologic features have been described in benign melanocytic lesions following cryotherapy. These atypical features include loss of maturation and increased staining with HMB-45, which could make the differentiation of benign from malignant melanocytic lesions difficult. 
AIDS-related Kaposi sarcoma can be treated by performing two 30-second freeze-thaw cycles with 3-mm margins every 4 weeks.
Capillary hemangioma can be treated with two 30-second freeze-thaw cycles with a 1-mm margin.
Cysts and tumors
One 10-second freeze-thaw cycle with a 1-mm margin can be used to treat acne cysts. This method is usually adequate to cause exfoliation and to open pores.
For milia, a short freeze-thaw cycle of 5-10 seconds is usually adequate.
Skin tags can be treated with one 10-second freeze-thaw cycle.
Seborrheic keratosis can be treated with one 10-second freeze-thaw cycle.
One 15- to 30-second freeze-thaw cycle with a 1-mm margin can be used to treat keloids.  Cryotherapy of keloids can be painful. Other modalities, such as intralesional corticosteroid injection, are more commonly used.
Rhinophyma can be treated with two 30-second freeze-thaw cycles of the entire nose at 4-week intervals. 
The freeze time for actinic keratoses is highly variable, depending on skin temperature and the thickness of the lesion. The combination of field-directed therapy and cryotherapy reportedly is more effective than cryotherapy alone. [16, 17]
Warts can usually be treated with two 15- to 30-second freeze-thaw cycles, depending on the thickness; however, some suggest that duct tape may be a more cost-effective and equally effective removal method. 
In a study of 74 children with molluscum contagiosum, imiquimod cream 5% was compared with cryotherapy. Cryotherapy was more rapid but was associated with more significant adverse effects (bullae formation, pigmentary changes, pain, superficial scarring). The effects of imiquimod treatment were of slower-onset but the treatment was virtually free of adverse effects. The authors suggest that in children, imiquimod may be better for numerous small lesions and cryotherapy may be better for large, solitary lesions. 
Cryotherapy reportedly is an effective treatment for epidermal nevi. Success was achieved with 2 cycles using an open-spray technique at 10-15 seconds each. Ten patients had successful results after 2-5 sessions, with no scarring. One patient had a relapse after 8 months, and 1 patient developed hypochromic scarring that resolved after 6 months. 
Lobomycosis is typically treated with surgical excision; however, in patients with multifocal lesions, treatment with cryosurgery and long-term itraconazole has been used with success. In one study, 5 sessions of two 2-minute freeze cycles accompanied by oral itraconazole for 6 months led to complete resolution, sparing a surgical procedure. 
A novel use of cryotherapy is selective cryolipolysis. This is when fat cells are subjected to near-subzero temperatures via surface cooling to cause selective cell death of adipose cells without harming the overlaying skin or nerves and vasculature within the target area. It was first described in 2008 and was written about in a human population in 2009. [22, 23]
While evidence of achieving a decreased fat layer is suggested by changes in thickness via ultrasound measurements, the long-term results are not yet not fully elucidated; this technology received FDA approval in 2010 (ZELTIQ, CoolSculpting; Pleasanton, Calif). However, the latest evidence indicates a robust patient response (86% saw improvement) with a limited adverse effect profile. Typically, only minimal discomfort occurred. Expected adverse effects are temporary erythema, bruising, and transient numbness, which usually resolve within 14 days of treatment. The most common serious adverse effect is late-onset pain (in 0.1%), occurring 2 weeks after the procedure. This seems to resolve without intervention. 
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