Difference between revisions of "Small vessel leukocytoclastic vasculitis"
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| Width = | | Width = | ||
| Caption = Leukocytoclastic vasculitis. [[H&E stain]]. | | Caption = Leukocytoclastic vasculitis. [[H&E stain]]. | ||
| Synonyms = | | Synonyms = leukocytoclastic vasculitis, hypersensitivity vasculitis | ||
| Micro = small vessels intramural inflammatory cells (neutrophils), vessel damage (fibrin deposition) | | Micro = small vessels intramural inflammatory cells (neutrophils), vessel damage (fibrin deposition) | ||
| Subtypes = | | Subtypes = | ||
| LMDDx = | | LMDDx = [[dermatitides with perivascular inflammation]] | ||
| Stains = PAS -ve | | Stains = [[PAS stain|PAS]] -ve | ||
| IHC = | | IHC = | ||
| EM = | | EM = | ||
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| Prognosis = dependent on underlying cause | | Prognosis = dependent on underlying cause | ||
| Other = | | Other = | ||
| ClinDDx = | | ClinDDx = see ''etiology'' section | ||
| Tx = | | Tx = remove underlying cause; colchicine and/or dapsone; immunosuppression | ||
}} | }} | ||
'''Small vessel leukocytoclastic vasculitis''', also '''leukocytoclastic vasculitis''' (abbreviated '''LCV'''), is an inflammatory process of the small [[blood vessel]]. | '''Small vessel leukocytoclastic vasculitis''', also '''leukocytoclastic vasculitis''' (abbreviated '''LCV''') and '''hypersensitivity vasculitis''',<ref name=pmid26176572>{{Cite journal | last1 = Einhorn | first1 = J. | last2 = Levis | first2 = JT. | title = Dermatologic Diagnosis: Leukocytoclastic Vasculitis. | journal = Perm J | volume = 19 | issue = 3 | pages = 77-8 | month = | year = 2015 | doi = 10.7812/TPP/15-001 | PMID = 26176572 }}</ref> is an inflammatory process of the small [[blood vessel]]. | ||
==General== | ==General== | ||
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*Palpable purpura, usu. lower extremity. | *Palpable purpura, usu. lower extremity. | ||
== | Treatment - dependent on cause - may include:<ref name=pmid24756249>{{Cite journal | last1 = Goeser | first1 = MR. | last2 = Laniosz | first2 = V. | last3 = Wetter | first3 = DA. | title = A practical approach to the diagnosis, evaluation, and management of cutaneous small-vessel vasculitis. | journal = Am J Clin Dermatol | volume = 15 | issue = 4 | pages = 299-306 | month = Aug | year = 2014 | doi = 10.1007/s40257-014-0076-6 | PMID = 24756249 }}</ref> | ||
*Remove underlying cause if it can be determined. | |||
* | *Colchicine and/or dapsone. | ||
*Immunosuppression. | |||
* | |||
* | |||
===Etiology=== | |||
Has a very broad DDx:<ref name=pmid18948765/> | Has a very broad DDx:<ref name=pmid18948765/> | ||
#Infectious: | #Infectious: | ||
Line 52: | Line 51: | ||
#Vasculitic disorders: | #Vasculitic disorders: | ||
#*ANCA mediated vasculitides: | #*ANCA mediated vasculitides: | ||
#**[[Wegener granulomatosis | #**[[Granulomatosis with polyangiitis]] (Wegener granulomatosis). | ||
#**[[Churg-Strauss syndrome | #**[[Eosinophilic granulomatosis with polyangiitis]] (Churg-Strauss syndrome). | ||
#*[[Henoch–Schönlein purpura]].<ref name=pmid9713395>{{Cite journal | last1 = Kraft | first1 = DM. | last2 = Mckee | first2 = D. | last3 = Scott | first3 = C. | title = Henoch-Schönlein purpura: a review. | journal = Am Fam Physician | volume = 58 | issue = 2 | pages = 405-8, 411 | month = Aug | year = 1998 | doi = | PMID = 9713395 }}</ref> | #*[[Henoch–Schönlein purpura]].<ref name=pmid9713395>{{Cite journal | last1 = Kraft | first1 = DM. | last2 = Mckee | first2 = D. | last3 = Scott | first3 = C. | title = Henoch-Schönlein purpura: a review. | journal = Am Fam Physician | volume = 58 | issue = 2 | pages = 405-8, 411 | month = Aug | year = 1998 | doi = | PMID = 9713395 }}</ref> | ||
#*Urticarial vasculitis. | #*Urticarial vasculitis. | ||
Line 61: | Line 60: | ||
#*Paraneoplastic. | #*Paraneoplastic. | ||
#*Drugs. | #*Drugs. | ||
==Gross== | |||
*Palpable purpura - raised lesions that can appreciated with touch, red/purple in colour. | |||
==Microscopic== | |||
Features:<ref name=pmid18948765/> | |||
*Small upper dermis vessels with: | |||
*#Neutrophils. | |||
*#*Fragmentation of [[neutrophil]]s (leukocytoclasia). | |||
*#Vessel damage: fibrin deposition (bright pink acellular stuff) or "nuclear dust" (punctate hyperchromatic material). | |||
DDx: | |||
*[[Dermatitides with perivascular inflammation]]. | |||
===Image=== | ===Image=== | ||
Line 77: | Line 89: | ||
==Stains== | ==Stains== | ||
*[[PAS stain|PAS]] - look for fungus. | *[[PAS stain|PAS]] - look for fungus. | ||
==Sign out== | |||
<pre> | |||
Skin, Left Outer Thigh, Punch Biopsy: | |||
- Hypersensitivity vasculitis (leukocytoclastic vasculitis). | |||
</pre> | |||
===Alternate=== | |||
<pre> | |||
Skin, Right Leg, Punch Biopsy: | |||
- Leukocytoclastic vasculitis. | |||
</pre> | |||
===Micro=== | |||
The sections show red blood cells extravasation and nuclear dust. Scattered neutrophils are within the wall of small blood vessels. | |||
==See also== | ==See also== | ||
*[[Vasculitides]]. | *[[Vasculitides]]. | ||
*[[Inflammatory skin disorders]]. | |||
==References== | ==References== |
Latest revision as of 16:56, 3 January 2019
Small vessel leukocytoclastic vasculitis | |
---|---|
Diagnosis in short | |
Leukocytoclastic vasculitis. H&E stain. | |
| |
Synonyms | leukocytoclastic vasculitis, hypersensitivity vasculitis |
| |
LM | small vessels intramural inflammatory cells (neutrophils), vessel damage (fibrin deposition) |
LM DDx | dermatitides with perivascular inflammation |
Stains | PAS -ve |
Site | blood vessels - see vasculitides |
| |
Signs | palpable purpura |
Prevalence | uncommon |
Prognosis | dependent on underlying cause |
Clin. DDx | see etiology section |
Treatment | remove underlying cause; colchicine and/or dapsone; immunosuppression |
Small vessel leukocytoclastic vasculitis, also leukocytoclastic vasculitis (abbreviated LCV) and hypersensitivity vasculitis,[1] is an inflammatory process of the small blood vessel.
General
- Most common cutaneous vasculitis.[2]
Clinical:
- Palpable purpura, usu. lower extremity.
Treatment - dependent on cause - may include:[3]
- Remove underlying cause if it can be determined.
- Colchicine and/or dapsone.
- Immunosuppression.
Etiology
Has a very broad DDx:[2]
- Infectious:
- Bacterial.
- Viral.
- Fungal.
- Vasculitic disorders:
- ANCA mediated vasculitides:
- Granulomatosis with polyangiitis (Wegener granulomatosis).
- Eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome).
- Henoch–Schönlein purpura.[4]
- Urticarial vasculitis.
- ANCA mediated vasculitides:
- Other:
- Connective tissue disease, e.g. mixed connective tissue disease, SLE, rheumatoid arthritis.
- Cryoglobulinemia - may be due to multiple myeloma, hepatitis C; have intravascular thrombi.
- Paraneoplastic.
- Drugs.
Gross
- Palpable purpura - raised lesions that can appreciated with touch, red/purple in colour.
Microscopic
Features:[2]
- Small upper dermis vessels with:
- Neutrophils.
- Fragmentation of neutrophils (leukocytoclasia).
- Vessel damage: fibrin deposition (bright pink acellular stuff) or "nuclear dust" (punctate hyperchromatic material).
- Neutrophils.
DDx:
Image
Case
www
Stains
- PAS - look for fungus.
Sign out
Skin, Left Outer Thigh, Punch Biopsy: - Hypersensitivity vasculitis (leukocytoclastic vasculitis).
Alternate
Skin, Right Leg, Punch Biopsy: - Leukocytoclastic vasculitis.
Micro
The sections show red blood cells extravasation and nuclear dust. Scattered neutrophils are within the wall of small blood vessels.
See also
References
- ↑ Einhorn, J.; Levis, JT. (2015). "Dermatologic Diagnosis: Leukocytoclastic Vasculitis.". Perm J 19 (3): 77-8. doi:10.7812/TPP/15-001. PMID 26176572.
- ↑ 2.0 2.1 2.2 Brinster, NK. (Nov 2008). "Dermatopathology for the surgical pathologist: a pattern-based approach to the diagnosis of inflammatory skin disorders (part II).". Adv Anat Pathol 15 (6): 350-69. doi:10.1097/PAP.0b013e31818b1ac6. PMID 18948765.
- ↑ Goeser, MR.; Laniosz, V.; Wetter, DA. (Aug 2014). "A practical approach to the diagnosis, evaluation, and management of cutaneous small-vessel vasculitis.". Am J Clin Dermatol 15 (4): 299-306. doi:10.1007/s40257-014-0076-6. PMID 24756249.
- ↑ Kraft, DM.; Mckee, D.; Scott, C. (Aug 1998). "Henoch-Schönlein purpura: a review.". Am Fam Physician 58 (2): 405-8, 411. PMID 9713395.