Other Lesions Flashcards

1
Q

What is this and how do you treat it?

A

Xanthelsmata (local accumulation of lipid deposits in eyelids)
Rx: surgical excision traditional w/ good cosmetic outcomes. Can do cryotherapy, laser ablation, chemical peels

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2
Q

What is an effective management strategy for keloids?

A

Keloid excision followed by radiation therapy performed within 1-3 days after surgery (10 and 15 Gy given over 2-3 days).

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3
Q

Describe the appearance/ characterization of hidradenitis supurrativa and cause.

A
  • Characterized by recurrent nodules and abscesses, typically of apocrine gland-bearing skin
    • can advance to large areas of abscesses and subcutaneous scarring and draining sinus tracts
    • Axillary, inguinal, perianal, and perineal most common. Lesions correspond with the milk line pattern of apocrine-related mammary tissue
  • Mechanism: follicular occlusion - hair follicles become occluded due to an overproliferation of ductal keratinocytes, rupture, and subsequently re-epithelialize. As this cycle continues, sinus tracts that house bacteria and cause chronic, painful infections and inflammation that can involve the skin and subcutaneous structures including muscle, fascia, and lymph nodes.
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4
Q

Describe Hurley Classification for HA.

A
  • stage I as transient nonscarring inflammatory lesions
  • stage II as separate lesions consisting of recurrent abscesses with tunnel formation and scarring, and single or multiple lesions separated by normal-looking skin
  • stage III as coalescent lesions with tunnel formation, scarring and inflammation.
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5
Q

Describe Hidradentitis supurrativa treatment.

A
  • Weight loss, hygiene, wound care and antibiotics.
  • Topical and systemic antibiotics are still the mainstay of treatment for mild HS.
    • Antibiotics do offer relief by reducing the burden of abscesses and pustules in some, but recurrence is frequent.
    • First line: 1% topical Clindamycin applied BID
    • clindamycin +/- resorcinol
  • Moderate disease: oral antibiotics instead of topical
    • 500 mg tetracycline BID
    • Refractory disease&raquo_space; antibiody therapy or surgical intervention
  • Humira (adalimumab) FDA approved for moderate to severe disease where patients have required long-term antibiotics or rapid flares upon cessation of antibiotics.
  • Surgical intervention once failed medication management (after 6 weeks of antibiotics or rapid therapy). This includes Wide excision to reduce recurrence (reserved for severe disease) Skin grafting vs. local flap may be required to close.
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6
Q

What are the common signs and symptoms of a Pilar Cyst?

A

Firm, slow-growing subcutaneous nodules, commonly on the scalp

They are similar to epidermoid cysts. They originate from the outer root sheath of the hair shaft.

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7
Q

What type of epithelium lines a Pilar Cyst?

A

Stratified squamous epithelium

This epithelium undergoes keratinization.

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8
Q

What is a Cylindroma?

A

Benign adnexal tumors showing eccrine and apocrine differentiation

Commonly found on the scalp and face, more frequent in women.

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9
Q

What syndrome is associated with multiple cylindromas?

A

Brooke-Spiegler syndrome

This genetic condition is inherited in an autosomal dominant manner with variable penetrance.

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10
Q

What is the recommended treatment for Cylindroma?

A

Surgical excision with close postoperative follow-up

Due to high recurrence rates.

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11
Q

What is a Pilomatricoma?

A

A benign, slow-growing skin tumor of hair follicle origin

Also known as pilomatrixoma or calcifying epithelium of Malherbe.

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12
Q

What is the common age group for Pilomatricoma occurrence?

A

Most common in children, but found in all ages

Tends to develop in the head and neck region.

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13
Q

What gene mutation is related to Pilomatricoma?

A

CTNNB1 gene mutation

This mutation is implicated in the tumorigenesis of hair matrix cells.

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14
Q

What are the characteristics of a Pilomatricoma? Treatment?

A

Slow-growing, firm to touch, mildly tender, slightly bluish without ulceration

Malignancy is very rare but can transform into malignant pilomatric carcinoma.

Rx: excision

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15
Q

What is a Spiradenoma?

A

Well-differentiated, benign dermal neoplasms

Their origin is controversial, possibly from sweat glands or hair follicles.

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16
Q

What age group is most commonly affected by Spiradenomas? How do they present?

A

Patients between 15 to 35 years of age

They present as small, solitary, painful nodules that can grow several cm, often with bluish hue

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17
Q

What is the treatment for Spiradenoma?

A

Excision

If pathology confirms diagnosis, observe and reassure.

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18
Q

What is Microcystic Adnexal Carcinoma (MAC)? How does it present?

A

A slow-growing skin cancer primarily affecting the head and neck

It usually presents as a fleshy, plaque-like lesion.

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19
Q

What is the common misdiagnosis for MAC?

A

Basal or squamous cell carcinomas

MAC can have perineural invasion.

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20
Q

What is the typical treatment for MAC?

A

Complete circumferential, peripheral, and deep margin assessment, usually with Mohs micrographic surgery

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21
Q

What is Keratoacanthoma?

A

A low-grade malignancy resembling squamous cell carcinoma (SCC)

It typically has a rapid growth followed by spontaneous regression.

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22
Q

What is the clinical presentation of Keratoacanthoma?

A

Solitary papule that rapidly increases in size with a crateriform center

Can progress to SCC with metastasis, but most commonly spontaneously regresses over several months

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23
Q

What is Merkel Cell Carcinoma?

A

An aggressive neuroendocrine tumor

It presents in older, immunocompromised individuals in sun-exposed areas.

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24
Q

What are the clinical features/ presentation of Merkel Cell Carcinoma summarized by the acronym AEIOU?

A

Asymptomatic, expanding, immunosuppressed, older than 50 years, ultraviolet-exposed fair skin

80% secondary to polyomavirus, 20% secondary to UV damage

25
What is the treatment for Merkel Cell Carcinoma?
Wide local excision if tumor < 2 cm with 1-2 cm margins + SLNB + adjuvant radiation
26
What is a Sebaceous Nevus? How does it present?
Jadassohn nevus, a hamartoma arising from pilosebaceous units It can appear cerebriform, nodular, or verrucous. Presents as yellowish flat plaque on the scalp or face.
27
What is the risk of malignant degeneration for Sebaceous Nevus? What is the treatment?
Historically reported at 10-15%, more recently shown to be <1% (Most commonly BCC) D/t verrucous appearance at puberty >> full thickness excision in children > 3 yo
28
What is Nevus of Ota?
Acquired dermal melanocytes hamartoma causing bluish hyperpigmentation ## Footnote It affects the ophthalmic and maxillary divisions of the trigeminal nerve.
29
What is a necessary part of the work up in a patient with Nevus of Ota? The primary treatment for Nevus of Ota?
Obtain ophthalmologist evaluation d/t 10% association with ipsilateral glaucoma. Rx with Laser therapy - Q-switched laser with ruby (694 nm) is the most effective option.
30
What is Pyogenic Granuloma?
A rapidly growing, friable papule that bleeds easily ## Footnote Often appears after local trauma in childhood.
31
What is the treatment for Pyogenic Granuloma?
Excision ## Footnote It is characterized by neutrophils causing skin ulceration.
32
What is Pyoderma Gangrenosum?
A rare skin disorder often associated with inflammatory bowel diseases ## Footnote It is believed to be immune-related and can appear after minor trauma.
33
What are the common signs and symptoms of Pyoderma Gangrenosum?
Starts as an erythematous plaque, may rapidly become a necrotizing ulcer with irregular borders Characterized by systemic inflammation and laboratory abnormalities (leukocytosis, hyponatremia, hypoproteinemia)
34
What is the initial treatment for Pyoderma Gangrenosum?
Medical treatment such as systemic steroids or immunosuppression ## Footnote Surgical intervention is reserved as a last resort.
35
What is the clinical resemblance of postoperative PG?
Necrotizing infection ## Footnote High index of suspicion is required for diagnosis.
36
What supports the diagnosis of PG?
Presence of neutrophilic dermatosis
37
What are the initial treatments for PG?
Systemic steroids or immunosuppression (and topical tacrolimus)
38
What is the characteristic appearance of Seborrheic Keratoses?
Well circumscribed, scaly, and stuck on appearance
39
What do Seborrheic Keratoses arise from?
Basal layer of the epidermis
40
What are the histological features of Seborrheic Keratoses?
* Hyperkeratosis * Acanthosis * Papillomatosis
41
Do Seborrheic Keratoses have malignant potential?
No malignant potential
42
What is a Glomus Tumor?
Benign hamartoma originating from the glomus body
43
What symptoms are associated with Glomus Tumor?
* Pain * Point tenderness * Sensitivity to cold
44
What imaging modality is most accurate for diagnosing Glomus Tumor?
MRI shows bright discrete mass on T2
45
What is the treatment for Glomus Tumor?
Excision
46
What condition does Rhinophyma occur with?
Progressive acne rosacea
47
What is the characteristic appearance of Rhinophyma?
Bulbous appearance due to sebaceous gland overgrowth
48
What is the first-line treatment for mild Rhinophyma? Advanced rhinophyma?
Topical and oral antibiotics with isoretinoin Advanced - tangential excision with secondary epithelialization or CO2 laser vs. dermabrasion
49
What is the most common type of soft tissue sarcoma?
Dermatofibrosarcoma Protuberans (DFSP)
50
What is a key characteristic of DFSP?
Latency in initial detection and slow infiltrative growth locally aggressive abdominal wall tumor with low metastatic potential. DFSP originates from cutaneous tissues and is limited to superficial structures. The majority of abdominal wall DFSP occur in adults aged 20 to 50 years with similar sex distribution, and tumors are small (<5 cm) with characteristic purple or blue discoloration.
51
Where is DFSP most commonly found?
Trunk > proximal extremities
52
What is the recommended treatment for DFSP?
Mohs (lower recurrence rate at 10% than WLE)
53
What is Xeroderma Pigmentosum?
AR disorder demonstrating defective DNA repair
54
What is the most common defect in Xeroderma Pigmentosum?
Mutations in nucleotide excision repair (NER) enzymes
55
What is the average age of diagnosis for nonmelanoma skin cancer in XP patients?
8 to 9 years old
56
What is a Dermatofibroma?
Benign nodule derived from mesodermal and dermal cells
57
Where are Dermatofibromas most commonly found?
Anterior surface of the lower legs
58
What is the Fitzpatrick sign associated with Dermatofibromas?
Dimpling or retraction of the lesions beneath the skin
59
What is the recommended treatment for Dermatofibromas?
Excisional biopsy