Difference between revisions of "Pityriasis rubra pilaris"
Jump to navigation
Jump to search
(tweak, wikify) |
|||
Line 52: | Line 52: | ||
*Occasional mild spongiosis. | *Occasional mild spongiosis. | ||
Notes: | |||
*PRP is easy to miss - clinical history (r/o PRP) usually needed to prompt correct diagnosis. | *PRP is easy to miss - clinical history (r/o PRP) usually needed to prompt correct diagnosis. | ||
*Psoriasis vulgaris <ref name=pmid18418089>{{Cite journal | last1 = Brinster | first1 = NK. | title = Dermatopathology for the surgical pathologist: a pattern based approach to the diagnosis of inflammatory skin disorders (part I). | journal = Adv Anat Pathol | volume = 15 | issue = 2 | pages = 76-96 | month = Mar | year = 2008 | doi = 10.1097/PAP.0b013e3181664e8d | PMID = 18418089 }}</ref> - thinned suprapapillary plates, hypogranulosis, neutrophils in the stratum corneum, dilated papillary dermal blood vessels, acantholysis absent | |||
*Lichen simplex chronicus - usually a localized process, not a widespread process. | ===Microscopic DDx=== | ||
*[[Psoriasis vulgaris]]<ref name=pmid18418089>{{Cite journal | last1 = Brinster | first1 = NK. | title = Dermatopathology for the surgical pathologist: a pattern based approach to the diagnosis of inflammatory skin disorders (part I). | journal = Adv Anat Pathol | volume = 15 | issue = 2 | pages = 76-96 | month = Mar | year = 2008 | doi = 10.1097/PAP.0b013e3181664e8d | PMID = 18418089 }}</ref> - thinned suprapapillary plates, hypogranulosis, neutrophils in the stratum corneum, dilated papillary dermal blood vessels, acantholysis absent. | |||
*[[Lichen simplex chronicus]] - usually a localized process, not a widespread process. | |||
*Darier disease - acantholysis is prominent with corps ronds and grains, follicular plugging absent. | *Darier disease - acantholysis is prominent with corps ronds and grains, follicular plugging absent. | ||
*Pemphigus vulgaris - PRP with extensive acantholysis | *[[Pemphigus vulgaris]] - PRP with extensive acantholysis can mimic; [[immunofluorescence|IF]] will be negative in PRP. | ||
*Hailey-Hailey - | *[[Hailey-Hailey disease]] - falling brick wall pattern of acantholysis. | ||
*Seborrhoeic dermatitis - more spongiotic, often with neutrophils. | *Seborrhoeic dermatitis - more spongiotic, often with neutrophils. | ||
*[[ | *[[Dermatophytosis|Fungal infection]]. | ||
==Associated Diagnoses== | ==Associated Diagnoses== |
Revision as of 04:51, 30 September 2014
Pityriasis rubra pilaris | |
---|---|
Diagnosis in short | |
| |
LM | alterating orthokeratosis and parakeratosis (known as "checkerboard pattern"), marked uniform acanthosis with broad dermal papillae and broad epidermal ridges, , +/-eosinophils (common), follicular plugging, scattered foci of acantholysis (common), occasional mild spongiosis |
LM DDx | fungal infection, psoriasis, Darier disease, seborrhoeic dermatitis |
Stains | PASD -ve (to r/o fungal infections) |
Gross | salmon-coloured plaques, well-demarcated |
Site | skin - see inflammatory skin disorders |
| |
Associated Dx | HIV infection - recalcitrant PRP |
Clinical history | Classic adult - self-limited exfoliative, erythematous dermatitis that starts over the head and neck and extends downwards forming orange plaques with spared islands of normal skin, follicular hyperkeratosis, palmar involvement with orange hyperkeratosis |
Prevalence | uncommon |
Treatment | retinoids, methotrexate and others |
Pityriasis rubra pilaris, abbreviated PRP, is an uncommon inflammatory skin disorder.
General
- Uncommon.[1]
- Typically sporadic, may be familial.[2]
- Bimodal age distribution:[3]
- Children: <10 years.
- Adults: 40s and 50s.
Treatment:
- Retinoids, methotrexate and others.[3]
Gross
Microscopic
Features:[1]
- Alterating orthokeratosis and parakeratosis - known as "checkerboard pattern".
- Marked uniform acanthosis with broad dermal papillae and broad epidermal ridges.
- Follicular plugging.
- +/-Eosinophils (common).
- Scattered foci of acantholysis.[4]
- Occasional mild spongiosis.
Notes:
- PRP is easy to miss - clinical history (r/o PRP) usually needed to prompt correct diagnosis.
Microscopic DDx
- Psoriasis vulgaris[5] - thinned suprapapillary plates, hypogranulosis, neutrophils in the stratum corneum, dilated papillary dermal blood vessels, acantholysis absent.
- Lichen simplex chronicus - usually a localized process, not a widespread process.
- Darier disease - acantholysis is prominent with corps ronds and grains, follicular plugging absent.
- Pemphigus vulgaris - PRP with extensive acantholysis can mimic; IF will be negative in PRP.
- Hailey-Hailey disease - falling brick wall pattern of acantholysis.
- Seborrhoeic dermatitis - more spongiotic, often with neutrophils.
- Fungal infection.
Associated Diagnoses
- HIV infection - recalcitrant PRP.
Images
Stains
See also
References
- ↑ 1.0 1.1 Marrouche, N.; Kurban, M.; Kibbi, AG.; Abbas, O. (Apr 2014). "Pityriasis rubra pilaris: clinicopathological study of 32 cases from Lebanon.". Int J Dermatol 53 (4): 434-9. PMID 24783259.
- ↑ Mercer, JM.; Pushpanthan, C.; Anandakrishnan, C.; Landells, ID.. "Familial pityriasis rubra pilaris: case report and review.". J Cutan Med Surg 17 (4): 226-32. PMID 23815954.
- ↑ 3.0 3.1 3.2 Klein, A.; Landthaler, M.; Karrer, S. (2010). "Pityriasis rubra pilaris: a review of diagnosis and treatment.". Am J Clin Dermatol 11 (3): 157-70. doi:10.2165/11530070-000000000-00000. PMID 20184391.
- ↑ 4.0 4.1 4.2 Leger, M.; Newlove, T.; Robinson, M.; Patel, R.; Meehan, S.; Ramachandran, S. (Dec 2012). "Pityriasis rubra pilaris.". Dermatol Online J 18 (12): 14. PMID 23286804.
- ↑ Brinster, NK. (Mar 2008). "Dermatopathology for the surgical pathologist: a pattern based approach to the diagnosis of inflammatory skin disorders (part I).". Adv Anat Pathol 15 (2): 76-96. doi:10.1097/PAP.0b013e3181664e8d. PMID 18418089.