Pathology of Melanocytic Tumors E-Book
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Pathology of Melanocytic Tumors E-Book

Klaus J. Busam, Richard A Scolyer, Pedram Gerami

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eBook - ePub

Pathology of Melanocytic Tumors E-Book

Klaus J. Busam, Richard A Scolyer, Pedram Gerami

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Constituting a large percentage of everyday diagnostic practice, melanocytic pathology is a complex and challenging area with many difficult-to-diagnose lesions. This highly illustrated reference, written by three of the world's leading dermatopathologists, provides authoritative guidance in the accurate diagnosis of even the most challenging pigmented skin tumors, helping you avoid pitfalls and recognize mimics.

  • Covers nearly every variant of melanocytic tumors you're likely to see.
  • Emphasizes how to arrive at an efficient, accurate diagnosis, and includes dermoscopic findings for optimal diagnostic precision.
  • Discusses modern analytic techniques ( cytogenetics, molecular studies ) and how to use them for diagnosis.
  • Includes numerous case examples to illustrate the differential diagnoses and work-up; how to use ancillary techniques, along with their pros, cons, and limitations; and clinical follow-up.
  • Presents the knowledge and experience of Klaus Busam, Pedram Gerami, and Richard Scolyer, – three dermatopathologists who are globally renowned for their expertise in melanoma pathology and analysis of melanocytic tumors by modern ancillary diagnostic techniques.

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Informations

Éditeur
Elsevier
Année
2018
ISBN
9780323508681
Sujet
Medizin
Sous-sujet
Pathologie
Section I
Benign Cutaneous Melanocytic Proliferations

Introduction

  1. 1. Melanotic Macules, 2
    • Klaus J. Busam
  2. 2. Acquired Melanocytic Nevi, 8
    • Pedram Gerami and Klaus J. Busam
  3. 3. Congenital Melanocytic Nevi, 26
    • Pedram Gerami
  4. 4. Spitz Nevi, 37
    • Pedram Gerami and Klaus J. Busam
  5. 5. Blue Nevi and Dermal Melanocytosis, 61
    • Klaus J. Busam
  6. 6. Deep Penetrating Nevi, 80
    • Klaus J. Busam, Iwei Yeh, and Richard A. Scolyer
  7. 7. Melanocytic Nevi of Special Sites, 90
    • Timothy VandenBoom and Pedram Gerami
  8. 8. Persistant/Recurrent Melanocytic Nevi, Traumatized Nevi, and Nevi Changing Under Therapy, 101
    • Maija Kiuru, Pedram Gerami, and Klaus J. Busam
  9. 9. Combined Melanocytic Nevi, 112
    • Klaus J. Busam and Richard A. Scolyer
  10. 10. Pigmented Epithelioid Melanocytoma, 124
    • Artur Zembowicz, Jarish N. Cohen, and Philip E. LeBoit
1

Melanotic Macules

Klaus J. Busam
The term melanotic macule is used to refer to benign flat pigmented lesions, which are histopathologically characterized by melanin pigment deposited in basilar keratinocytes without or at times with a slight increase in the density of solitary units of junctional melanocytes. Cutaneous and mucosal melanotic macules are often labeled lentigo. The conjunctival equivalent has historically been termed acquired melanosis. In contrast to melanocytic nevi, there are no junctional nests in melanotic macules, lentigines, or benign acquired melanosis. The lesions differ from melanoma in situ clinically by a tendency toward small size and sharp circumscription and histopathologically by a low density of melanocytes. Melanotic macules are a common clinical presentation. They are benign and do not need to be treated. However, they may be biopsied when they display irregular features, are new, or are changing, to exclude melanoma in situ.

Solar Lentigo

Clinical Features

Solar lentigo manifests as a discrete pigmented macule or patch on sun-exposed skin of middle-aged or elderly individuals (Box 1.1).1 Its color may range from light tan to dark brown. A lesion's color may be uniform or heterogeneous. The size of a solar lentigo may be small (2 mm) or large (>1 cm). Its peripheral borders may be regular or ill-defined (Figs. 1.1 and 1.2). Multiple lesions of solar lentigo may coexist in the same anatomic region. They may collide with each other or with seborrheic or actinic keratoses, become confluent, and appear clinically complex. Clinical atypical lesions, which stand out from the background, prompt concerns for lentigo maligna (melanoma in situ) and are usually biopsied to assess for or exclude melanoma. Solar lentigines become more frequent and/or larger in area with age. Lesions of solar lentigo can also be found in young patients with sun-damaged skin and are common in children with xeroderma pigmentosum.
Box 1.1
Solar Lentigo
Clinical Findings
  • Usually adults
  • Men > women
  • Predominantly whites
  • Pigmented macule or patch
  • Often in sun-exposed areas
Histopathology
  • Basal layer hyperpigmentation
  • Normal density of melanocytes or solar melanocyte hyperplasia
  • No cytologic atypia
  • May be inflamed
  • May be associated with melanophages
Differential Diagnosis
  • Pigmented actinic keratosis
  • Macular pigmented seborrheic keratosis
  • Lichenoid keratosis
  • Lentigo simplex
  • Melanoma in situ
image

Fig. 1.1 Clinical Appearance of Solar Lentigo. (A) Pigmented macule. (B) This lesion is small but irregular in outline. Its asymmetric silhouette was the reason why it was biopsied.
image
image
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Fig. 1.2 Clinical Appearance of Solar Lentigo. (A) Hyperpigmented macule in a background of light brown macules on the chest of an elderly woman. (B) The lesion displays some irregular borders and variation in pigment intensity. (C) Corresponding dermoscopic findings.
A variant of solar lentigo clinically characterized by presentation as small dark macules, especially on the upper back, has been referred to as “ink spot” lentigo or reticulated melanotic macule.2

Histopathologic Findings

Solar lentigo is histopathologically characterized by hypermelanization of basilar keratinocytes (Figs. 1.3–1.5). Often there is associated slight epidermal hyperplasia resulting in elongated, club-shaped rete ridges. As rete ridges become longer, they may form a reticulate pattern. Lesions of solar lentigo may be associated with or develop into a seborrheic keratosis (Fig. 1.6). Pigmentation of keratinocytes is then typically most pronounced at the tip of rete ridges. In some lesions the rete ridges may...

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