Clinical History: Papule on thigh of a 50 year

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1. Clinical History: Papule on thigh of a 50 year-old male
Choose the correct diagnosis:
a. Clear cell acanthoma
b. Large cell acanthoma
c. Poroma
d. Psoriasis
Correct Answer: a
Histologic Description: There is a markedly acanthotic epidermis with neutrophilic spongiosis,
parakeratosis with neutrophils, and hypogranulosis. The keratinocytes have a clear cytoplasm and the
lesion is well demarcated from the adjacent normal epidermis.
Discussion:
Clear cell acanthoma is a benign epidermal lesion that clinically presents as an erythematous
plaque or nodule on the lower leg. It can have a collaret of scale and weep clear fluid. Histologically, one
sees epidermal acanthosis with hypogranulosis, parakeratosis, and neutrophilic spongiosis. Neutrophils
can also be noted in the parakeratotic scale. The lesion is well demarcated from the surrounding
epidermis and the keratinocytes, as the name suggests, take on a clear appearance due to the
accumulation of glycogen. One can note dilated capillaries in the superficial papillary dermis as well.
Large cell acanthoma lacks the clear keratinocytes, parakeratosis, and inflammatory infiltrate. The
lesion, usually, is usually well demarcated with large keratinocytes, but lacks significant nuclear atypia.
There can be hypergranulosis, in contrast to a clear cell acanthoma. On low power, a poroma would
have an acanthotic epidermis with a proliferation of monomorphic cuboidal or basaloid cells exhibiting
ductal differentiation. Although psoriasis has hypogranulosis and neutrophilic parakeratosis, it does not
show such striking demarcation from the surrounding normal epidermis and it has a thinning of the
supra-papillary plates, dilated capillaries, and elongation of the rete ridges. In addition, psoriasis does
not usually present as a single lesion.
2. Clinical History: 60 year-old female with a thigh mass
Choose the correct diagnosis:
a. Angiosarcoma
b. Intravascular Papillary Endothelial Hyperplasia
c. Lobular Capillary Hemangioma (pyogenic granuloma)
d. Solitary Fibrous Tumor
Correct Answer: c
Histologic Description: In the deep reticular dermis, one sees a well circumscribed lobulated collection
of thin walled vessels in a fibrotic stroma. The epidermis is unremarkable. Nuclear atypia and mitoses
are not seen.
Discussion:
Pyogenic granuloma is a benign, reactive vascular proliferation which occurs in response to
trauma. It is commonly seen on the head and neck or distal extremities. It is not uncommon in the
pediatric population and gingival lesions can occur in pregnancy. Clinical presentation is usually that of a
juicy, erythematous, friable papule or nodule that bleeds easily. They can occur deep within the skin and
have a violaceous color, which may be mistaken for melanoma. Histologically, they typically occur in the
papillary dermis, but they can occur in the reticular dermis or intravascularly. The lesion has a well
circumscribed collection of thin walled capillaries that can take on a lobulated appearance. Superficial
lesions have a collarette of scale. The surrounding stroma may have a myxoid and edematous
appearance with occasional mast cells and stellate fibroblasts. Fibrosis may be seen in involuting lesions.
Angiosarcoma would show a poorly formed vessels dissecting between collagen fibers in the dermis
with prominent nuclear atypia and mitoses. Intravascular papillary endothelial hyperplasia would not
show such well formed vessels and can be associated with a thrombus within a larger vessel. A solitary
fibrous tumor shows a proliferation of spindle cells in a pattern-less pattern associated with staghorn
vessels.
3. Clinical History: 15 year-old female with a papule on the chin
Choose the correct answer:
a. Dermatofibroma (Fibrous Histiocytoma)
b. Juvenile Xanthogranuloma
c. Necrobiotic Xanthogranuloma
d. Xanthoma
Correct Answer: b
Histologic Description: Beneath a normal epidermis one sees a collection of foamy histiocytes
and giant cells with a wreath-like configuration of nuclei.
Discussion:
Juvenile Xanthogranuloma (JXG) is a benign histiocytic lesion that usually occurs in childhood
and presents as a reddish-brown papule involving the head and neck area, but other sites can be
involved. Multiple lesions may be associated with neurofibromatosis and juvenile chronic
myelogenous leukemia. Visceral involvement may occur, but this is rare. Histologically, one
typically sees a well circumscribed dome shaped lesion in the superficial dermis consisting of
foamy histiocytes and giant cells that have nuclei in a wreath configuration (Touton giant cells).
Neutrophils, lymphocytes, and eosinophils may be interspersed throughout the lesion.
Necrobiotic xanthogranuloma (NXG) may show Touton like giant cells, but one usually
sees striking necrobiotic change throughout the dermis associated with extracellular cholesterol
deposits. NXG typically presents in adults and is associated with monoclonal gammopathy.
Xanthomas have foamy histiocytes, but lack Touton giant cells. Although dermatofibromas may
have xanthomatized histiocytes, they usually have the characteristic collagen wrapping
configuration associated with peudoepitheliomatous hyperplasia and basal layer
hyperpigmentation.
4. Clinical History: 60 year-old male with a papule on the nose
Choose the correct answer:
a. Inverted Follicular Keratosis
b. Squamous Cell Carcinoma
c. Trichilemmoma
d. Verruca Vulgaris
Correct Answer: c
Histologic Description: There is a markedly acanthotic epidermis with clear keratinocytes and
peripherally there one notes basaloid cells in a palisading pattern.
Discussion:
A trichilemmoma is a benign epidermal growth that derives from the follicular
infundibulum and shows outer root sheath differentiation. They are characteristically found on
the face and multiple lesions are associated with Cowden’s syndrome. Histologically, one sees a
well demarcated, lobulated epidermal proliferation of keratinocytes with cytoplasmic clearing
due to glycogen accumulation. The lesion is enveloped by basophilic columnar cells arranged in
a palisaded fashion and eosinophilic basement membrane mimicking the outer root sheath of
the hair follicle. Desmoplastic trichilemmomas are similar but are also accompanied by an
abutting desmoplastic stroma. A squamous cell carcinoma would show prominent nuclear
atypia and lacks the palisading of a trichilemmoma. Inverted follicular keratosis shows a
verrucoid lesion with whorls of glassy keratinocytes at the base. Verruca vulgaris is characterized
by koilocytes with pyknotic nuclei and cytoplasmic clearing commonly found in the expanded
granular layer.
5. Clinical History: 90 year old male with a mass in the axilla
Choose the correct answer:
a. Nodular hidradenoma (acrospiroma)
b. Sebaceous adenoma
c. Sebaceous carcinoma
d. Sebaceous epithelioma
Correct Answer: d
Histologic Description: Deep in the reticular dermis, one notes a well circumscribed tumor
consisting of basaloid cells. Occasional cells with a vacuolar cytoplasm that indents the nucleus
are seen. Scattered mitoses are seen, but the cells lack prominent nuclear atypia.
Discussion:
Sebaceous epithelioma (sebaceoma) is a sebaceous tumor that typically involves the
head and neck area. It clinically presents as yellowish nodule or plaque. Microscopically, they
consist of well circumscribed proliferation of lobules or nests of blue cells representing
immature sebocytes admixed with more differentiated cells showing clear sebaceous
differentiation. Typically more than half the lesion will consist of these immature germinative
cells. Mitoses can be found, but are not indicative of malignancy. Nuclear atypia is absent or
rare, and one should be suspicious of sebaceous carcinoma in more atypical lesions. Multiple
lesions can be associated with Muir-Torre syndrome. Sebaceous adenomas can show similar
histology, but the structure of the normal sebaceous gland is usually retained. In a sebaceous
adenoma the number of well differentiated sebaceous cells outnumbers the immature
sebocytes, which tend to be found at the periphery of the lesion and mature inwards. An
acrospiroma consists of lobules of blue cells with ductal differentiation admixed with cells that
have clear or squamoid differentiation. Nodular hidradenoma is thought to be eccrine of origin
and does not show sebaceous differentiation.
6. Clinical History: 80 year old male with a recent eruption of vesicles on the forearm
Choose the correct answer:
a. Coxsackie Virus infection
b. Herpes Simplex/Varicella Zoster Virus infection
c. Molluscum Contagiosum
d. Orf
Answer: b
Histologic Description: The epidermis shows marked reticular and ballooning degeneration.
Keratinocytes with steel gray nuclei and multi-nucleated giant cells are seen.
Discussion:
Herpes Simplex (Types 1 and 2) and Varicella Zoster virus have the same characteristic
histology. The main changes include: ballooning and reticular degeneration of the epidermis ( a
sign suggestive of viral disease), steel gray keratinocyte nuclear inclusions with margination of
the chromatin, multinucleated keratinocyte with nuclear molding, and leukocytoclastic vasculitis
in the papillary dermis. Coxsackie viruses (typically A16) are the cause of hand-foot-mouth
syndrome. The low power view is similar to HSV infection with prominent reticular and
ballooning degeneration, but multinucleated giant cells and nuclear inclusions are not seen.
Molluscum Contagiosum is a superficial Parapox infection with characteristic cytoplasmic
eosinophilic-basophilic inclusions (Henderson-Patterson bodies). Orf (ecthyma contagiosum) is a
Parapox infection acquired from sheep or goats. The lesion usually progresses through several
stages: macular, target, weeping, nodular, verrucous, and regressive. On histology, one notes
reticular degeneration with both cytoplasmic and nuclear eosinophilic inclusions (HSV is only
nuclear).
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