Ronald P. Rapini

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Ronald P. Rapini born 1954 in Akron, Ohio, is an American dermatologist and dermatopathologist. He is the Chernosky Distinguished Professor and Chair of the Department of Dermatology at the University of Texas Health Science Center at Houston and MD Anderson Cancer Center. [1]

Biography

He received his medical degree from Ohio State University in 1978 and did an internship at Marshfield Clinic (1978–1979) and Dermatology residency at the University of Iowa (1979–1982), as well as a fellowship at the University of Colorado Health Sciences Center (1982–1983). [2]

As department chair from 2002 to the present, he has led considerable growth in the dermatology program. The combined program at UTHSC and MD Anderson Cancer Center has 27 full time faculty, 21 dermatology residents, and 3 fellows as of July 2020. A number of his trainees went on to national recognition including receiving the AMA Foundation Leadership Award. [3]

He has served as the president of the American Board of Dermatology, the American Society of Dermatopathology, the American Society for Mohs Surgery, the Houston Dermatological Society, and the Texas Dermatological Society. [4] Several society awards have recognized his work, such as the Walter Nickel Award from the American Society of Dermatopathology for excellence in teaching in 2005. [5] He also received the Founder's Award from American Society of Dermatopathology, on October 12, 2012, and the Robert G. Freeman Mentoring and Leadership award from the Texas Dermatological Society, May 17, 2013

He is the sole author of the textbook Practical Dermatopathology (2005, Mosby), which is widely used around the world, and former lead co-editor of the two-volume text Dermatology (2nd. ed 2007, Mosby). The two-volume Dermatology is a primary clinical and training textbook used in many dermatology training programs and dermatology clinics across the world. [6] As of July 2020, he has published 142 peer-reviewed articles and has been a speaker at 473 meetings in the US and throughout the world. He has also authored 65 textbook chapters, including 3 chapters for emedicine. [7] [8] [9]

He described the first case of Swimmers itch to occur in exposed skin [10] and described the first case of herpetic paronychia occurring in an atopic patient while on isotretinoin therapy for acne. [11] He confirmed that the incidence of epidermolytic hyperkeratosis is higher in association with dysplastic nevi than in ordinary melanocytic nevi and may serve as a marker for nevus with architectural disorder. [11]

Related Research Articles

<span class="mw-page-title-main">Melanocytic nevus</span> Medical condition

A melanocytic nevus is usually a noncancerous condition of pigment-producing skin cells. It is a type of melanocytic tumor that contains nevus cells. Some sources equate the term mole with "melanocytic nevus", but there are also sources that equate the term mole with any nevus form.

<span class="mw-page-title-main">Nevus</span> Mole or birthmark; visible, circumscribed, chronic skin lesion

Nevus is a nonspecific medical term for a visible, circumscribed, chronic lesion of the skin or mucosa. The term originates from nævus, which is Latin for "birthmark"; however, a nevus can be either congenital or acquired. Common terms, including mole, birthmark, and beauty mark, are used to describe nevi, but these terms do not distinguish specific types of nevi from one another.

<span class="mw-page-title-main">Hyperkeratosis</span> Medical condition

Hyperkeratosis is thickening of the stratum corneum, often associated with the presence of an abnormal quantity of keratin, and also usually accompanied by an increase in the granular layer. As the corneum layer normally varies greatly in thickness in different sites, some experience is needed to assess minor degrees of hyperkeratosis.

<span class="mw-page-title-main">Dysplastic nevus</span> Medical condition

A dysplastic nevus or atypical mole is a nevus (mole) whose appearance is different from that of common moles. In 1992, the NIH recommended that the term "dysplastic nevus" be avoided in favor of the term "atypical mole". An atypical mole may also be referred to as an atypical melanocytic nevus, atypical nevus, B-K mole, Clark's nevus, dysplastic melanocytic nevus, or nevus with architectural disorder.

Keratoderma is a hornlike skin condition.

<span class="mw-page-title-main">Congenital melanocytic nevus</span> Congenital mole caused by genetic mutations

The congenital melanocytic nevus is a type of melanocytic nevus found in infants at birth. This type of birthmark occurs in an estimated 1% of infants worldwide; it is located in the area of the head and neck 15% of the time.

<span class="mw-page-title-main">Becker's nevus</span> Medical condition

Becker's nevus is a benign skin disorder predominantly affecting males. The nevus can be present at birth, but more often shows up around puberty. It generally first appears as an irregular pigmentation on the torso or upper arm, and gradually enlarges irregularly, becoming thickened and often hairy (hypertrichosis). The nevus is due to an overgrowth of the epidermis, pigment cells (melanocytes), and hair follicles. This form of nevus was first documented in 1948 by American dermatologist Samuel William Becker (1894–1964).

<span class="mw-page-title-main">Nevus of Ota</span> Human facial birthmark

Nevus of Ota is a hyperpigmentation that occurs on the face, most often appearing on the white of the eye. It also occurs on the forehead, nose, cheek, periorbital region, and temple.

<span class="mw-page-title-main">Blue nevus</span> Type of melanocytic tumor

A blue nevus is a type of coloured mole, typically a single well-defined blue-black bump.

Phakomatosis pigmentovascularis is a rare neurocutanous condition where there is coexistence of a capillary malformation with various melanocytic lesions, including dermal melanocytosis, nevus spilus, and nevus of Ota.

Ichthyosis hystrix is a group of rare skin disorders in the ichthyosis family of skin disorders characterized by massive hyperkeratosis with an appearance like spiny scales. This term is also used to refer to a type of epidermal nevi with extensive bilateral distribution.

<span class="mw-page-title-main">Nevus lipomatosus superficialis</span>

Nevus lipomatosus (cutaneous) superficialis is characterized by soft, yellowish papules or cerebriform plaques, usually of the buttock or thigh, less often of the ear or scalp, with a wrinkled rather than warty surface. It is usually congenital in origin or appears within the first three decades.

<span class="mw-page-title-main">Spitz nevus</span> Medical condition

A Spitz nevus is a benign skin lesion. A type of melanocytic nevus, it affects the epidermis and dermis.

Epidermal nevus syndrome is a rare disease that was first described in 1968 and consists of extensive epidermal nevi with abnormalities of the central nervous system (CNS), skeleton, skin, cardiovascular system, genitourinary system and eyes. However, since the syndrome's first description, a broader concept for the "epidermal nevus" syndrome has been proposed, with at least six types being described:

A benign melanocytic nevus is a cutaneous condition characterised by well-circumscribed, pigmented, round or ovoid lesions, generally measuring from 2 to 6 mm in diameter. A benign melanocytic nevus may feature hair or pigmentation as well.

Pseudomelanoma is a cutaneous condition in which melanotic skin lesions clinically resemble a superficial spreading melanoma at the site of a recent shave removal of a melanocytic nevus.

<span class="mw-page-title-main">Desmoplastic melanoma</span> Medical condition

Desmoplastic melanoma is a rare cutaneous condition characterized by a deeply infiltrating type of melanoma with an abundance of fibrous matrix. It usually occurs in the head and neck region of older people with sun-damaged skin. Diagnosis can be difficult as it has a similar appearance to sclerosing melanocytic nevi as well as some nonmelanocytic skin lesions such as scars, fibromas, or cysts.

Walter Russell "Nick" Nickel, M.D. was an American dermatologist who was one of the founders of the field of dermatopathology. He was a co-founder and president of four different professional societies and was the founding chairman of the Division of Dermatology at the University of California, San Diego Medical Center.

<span class="mw-page-title-main">Acral nevus</span> Medical condition

An acral nevus is a cutaneous condition of the palms, soles, fingers, or toes, characterized by a skin lesion that is usually macular or only slightly elevated, and may display a uniform brown or dark brown color, often with linear striations.

<span class="mw-page-title-main">Pigmented spindle cell nevus</span> Medical condition

A pigmented spindle cell nevus is a skin condition characterized by a dark brown to black macule or papule, usually less than 6 mm.

References

  1. Ronald P. Rapini M.D.: Executive Profile & Biography - Bloomberg
  2. [ University of Texas at Houston Medical Center - Department of Dermatology - Ronald P. Rapini
  3. Source (2004-03-28). "Manage Account - ModernMedicine". Dermatologytimes.modernmedicine.com. Retrieved 2011-01-02.
  4. "Ronald P. Rapini, MD, FAAD, Joins Board of Directors of the American Academy of Dermatology". Aad.org. Archived from the original on 2010-07-06. Retrieved 2011-01-02.
  5. "The American Society of Dermatopathology | Walter R. Nickel Award". ASDP. Archived from the original on 2010-12-03. Retrieved 2011-01-02.
  6. Dermatology, 2nd Edition - 2-Volume Set. Dermatology-s10.cdlib.org (2009-01-01). Retrieved on 2009-02-02.
  7. Multicentric Reticulohistiocytosis at eMedicine
  8. Fire Ant Bites at eMedicine
  9. Spitz Nevus at eMedicine
  10. Tremaine AM, Whittemore DE, Gewirtzman AJ, et al. (January 2009). "An unusual case of swimmer's itch". Journal of the American Academy of Dermatology. 60 (1): 174–6. doi:10.1016/j.jaad.2008.07.060. PMID   19103378.
  11. 1 2 Conlin PA, Rapini RP (February 2002). "Epidermolytic hyperkeratosis associated with melanocytic nevi: a report of 53 cases". The American Journal of Dermatopathology. 24 (1): 23–5. doi:10.1097/00000372-200202000-00004. PMID   11803276. S2CID   23244315.