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Dermatology Differential Diagnosis Guide

This document outlines the topics to be covered in a dermatology lecture, including a review of primary skin lesions and their differential diagnoses. The lecture will discuss macules, patches, papules, plaques, wheals, nodules, ulcers and blisters. Specific conditions that will be covered include systemic lupus erythematosus, exfoliative dermatitis, hyperpigmented and hypopigmented lesions, alopecia, purpura, urticaria, nodules, ulcers and blistering disorders. Clinical cases will also be viewed and discussed.

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0% found this document useful (0 votes)
20 views17 pages

Dermatology Differential Diagnosis Guide

This document outlines the topics to be covered in a dermatology lecture, including a review of primary skin lesions and their differential diagnoses. The lecture will discuss macules, patches, papules, plaques, wheals, nodules, ulcers and blisters. Specific conditions that will be covered include systemic lupus erythematosus, exfoliative dermatitis, hyperpigmented and hypopigmented lesions, alopecia, purpura, urticaria, nodules, ulcers and blistering disorders. Clinical cases will also be viewed and discussed.

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Dermatology Lecture 5-21-09

by Ma. Socorro W. Toledo, MD,FPDS

To the third year medical student:


• After the 2nd year PD lecture, this session aims to
bridge that discussion of skin lesions with
diagnosis of specific diseases.
• Review the PD concepts.
• Familiarize yourself with the diseases mentioned
in this handout.
• We will view and discuss actual clinical cases.
• We start promptly at 8 a.m.
Primary Skin Lesions and
Differential Diagnoses
(Ma. Socorro W. Toledo, MD, FPDS)

• Outline of Discussion According to Skin Lesion:


• I. Macules,Patches/ Papules,Plaques
• II. Wheals
• III. Nodules
• IV. Ulcers
• V. Blisters = Vesicles/ Bullae
I. Macules/Patches;
Papules/ Plaques
• A. SLE
• B. Exfoliative Dermatitis
• C. Hyperpigmented Lesions
• D. Hypopigmented Lesions
• E. Alopecia
• F. Purpura
• G. Leprosy
• H. Cutaneous Lymphoma (MF)
I. Macules/patches or
papules/plaques
A. Systemic Lupus
Erythematosus (SLE)
• 4/11 criteria: Malar rash, discoid rash,
photosensitivity, oral ulcers
• 11 criteria involve cutaneous(4),
musculoskeletal, hematologic, renal,
pulmonary, cardiac, immunologic,
nervous system abnormalities
Gilliam Classification of
LE skin lesions
1. LE-specific skin disease (cutaneous LE):
LE-specific on histopathology
• a. acute CLE– localized (malar or butterfly rash),
generalized erythema
• b. subacute CLE– annular, papulosquamous
• c. chronic CLE
i..classic discoid
ii. hypertrophic/verrucous
iii. lupus profundus or
lupus panniculitis
iv. Lupus tumidus (urticarial)
v. Mucosal dle – oral, conjunctival
Gilliam Classification of LE skin
lesions
2. LE-nonspecific skin disease:
Not LE-specific on histology
• Vasculitis
• Alopecia
• Bullae
• Leg ulcers
• Urticaria
• Nodules
• Acanthosis nigricans
Pathogenesis
• Triggers:
UV radiation, infection, drug and chemical
exposure, cigarette smoking

• Example of a mechanism:
UV light induces expression of “neoantigens” (i.e
intracellular antigens like Ro/SS-A,
La/ SS-B and calreticulin displaced to
keratinocyte cell surface)  target of a
dysregulated immune attack.
B. Exfoliative dermatitis
(Erythroderma)
• Characterized by erythema and extensive scaling of skin (70% or
more)
• Scaling may be thick or thin, of large sheets or small flakes of
skin, exudative or thickly crusted
• Constitutional signs and symptoms are present
• Chilliness  (+)inability of cutaneous blood vessels to constrict
• Hospitalization : For laboratory work-ups, proper therapeutics and
nutrition, patient convenience
• Varied etiologic factors: Inflammatory dses, Infectious dses,
Malignancies
• Skin biopsy by a dermatologist is IMPERATIVE
• Prognosis: Very good to grave depending on etiology
• Therapy : Months or years
C. Hyperpigmented Lesions
a. Post-inflammatory hyperpigmentation
b. Acanthosis nigricans
c. Amyloidosis –cutaneous/ systemic
d. Reaction to drugs (eg minocycline) heavy
metals, exogenous agents
e. Congenital d/o: Mongolian spot
f. Idiopathic: Ashy dermatosis
D. Hypopigmented Lesions
• VITILIGO
• - Loss of melanocytes
• - Etiology(?): autoimmunity,
autocytotoxicity, neurohumoral factors
• – most often associated with diseases of
the thyroid gland (hypo/hyperthyroidism)
• - localized (focal, segmental, acrofacial) or
generalized
E. ALOPECIA
-Definition: Loss of hair
- Most common area: Scalp
- SLE – scarring or nonscarring alopecia
- Syphilis – “moth-eaten” appearance
- Other causes: anemia, thyroid disorders,
infections
- Idiopathic
F. PURPURA
- Extravasation of blood
- Nonblanching (as opposed to
telangiectasia)
Example:
Hypersensitivity Vasculitis
Etiologies: Infections, Drug Reactions
II. Wheals = Urticaria

A. Primary or idiopathic
B. Secondary Varied etiology:
1. contact urticaria
2. food
3. drugs
4. physical urticaria
5. infectious etiology - UTI, PTB, Hepatitis, HIV
6. systemic disease - SLE, hyperthyroidism
7. genetic origin - hereditary angioedema

8. malignancy
Physical urticaria

a. Pressure urticaria - [Link]


b. Solar urticaria
c. Heat urticaria
d. Cold urticaria
e. Exercise-induced urticaria
f. Vibration-induced urticaria
III. Nodules
a. Hereditary/ metabolic disorders
- Neurofibroma
- Xanthoma
- Myxedema (in hyperthyroidism)
b. Infection: Leprosy
c. Malignancy : leukemia/lymphoma cutis
d. Autoimmune disorders: SLE
e. Congenital malformations: hemangioma
f. Inflammatory d/o: Panniculitis
IV. Ulcers
a. Infection
b. Malignancy

c. Disorders of the circulatory system


1. Stasis ulcers 2* to venous insufficiency
2. Ulcers 2* to thromboembolism/ infarction

d. Metabolic diseases –
[Link] lipoidica diabeticorum
e. Idiopathic – e.g. pyoderma gangrenosum
V. Blistering disorders
a. Burns
b. Infection – viral, bacterial, fungal
c. Contact dermatitis

d. Autoimmune diseases –
Pemphigus, Bullous pemphigoid,
Epidermolysis bullosa, SLE

e. Endocrine diseases – diabetic bulla


f. Nutritional disorders - zinc deficiency

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