SUB CUTANEOUS
LEG NODULES:
When a doctor
sees a patient with subcutaneous leg nodules, he has various clinical condition
in mind. The problem is that without a
biopsy it is difficult to diagnose them.
Erythema nodosum can be diagnosed clinically from the location of
painful, red, slightly bruised nodules over the anterior shins and also
pretibial myxoedema can generally be diagnosed from the peau d’orange
appearance of mucin infiltrates on the anterior shin. However, a lot of other subcutaneous nodules
particularly on the calf, will require a deep biopsy to make the
diagnosis. Other considerations include
erythema induratum, pancreatic panniculitis, lupus panniculitis, subcutaneous
T-cell lymphoma, deep fungal infection and atypical bacterial infection. Under this layout the histopathology of these
various conditions and how to compare and contrast them. Other types of panniculitis to consider are
Alpha 1 antitrypsin deficiency and eosinophilic panniculitis. Lupus panniculitis typically gives overlying
skin atrophy, there is a deep indentation with fibrosis or subcutaneous fat
pulling the skin in.
Most patients
with infective causes are usually immunosuppressed either with HIV disease or
because they are on immunosuppressive drugs or chemotherapy.
Subcutaneous T-cell lymphomas are rare, both T and B cell lymphomas do involve the leg. The large B-cell lymphoma leg type or
subcutaneous T-cell lymphoma are the commonest.
Gamma Delta T-cell lymphoma usually presents as infiltrating eroding
plaques or tumours rather than subcutaneous nodules and it has a poor
prognosis.
Clinical - Large purple plaques on the skin surface or deeper nodules. The plaques may ulcerate.
Clinical - Large purple plaques on the skin surface or deeper nodules. The plaques may ulcerate.
Erythema nodosum is
usually widening of the septum with infiltrate of lymphocytes and some
neutrophils around the septal vessels with mild involvement of the periphery of
the fat lobules.
Erythema induratum
involves medium sized vessels with vasculitis and granulomatous inflammation
and necrosis. Sometimes the vascular
involvement has had this condition described as nodular vasculitis. Previously reaction to tuberculosis was the
commonest cause or erythema induratum.
Lupus panniculitis. Early
lesions have lobular lymphocytic infiltrate with plasma cells and there may be
lymphoid follicles formed. Mucin is also
deposited in the deep dermis and subcutaneous fat. With time the amount of mucin decreases and
collagen is deposited and ultimately develops a sclerosing panniculitis which
causes the indentation of the skin in these lesions.
Cutaneous polyarteritis nodosa. Usually a large
vessel is involved and initially the infiltrates neutrophilic while later it
becomes cystic cytic.
Panniculitis due to Alpha 1 Antitrypsin deficiency shows a neutrophilic infiltrate at the fat dermal junction so it is
not an obvious diagnosis.
Subcutaneous Sweet’s Syndrome may also give neutrophils.
This usually involves the fat and doesn’t give a superficial
infiltrate. The clinical lesions look
much the same as passive Sweet’s.
Pancreatic panniculitis
involves the lobules and gives liquid fat necrosis with ghost cells.
Eosinophilic panniculitis has
the fat infiltrated with eosinophils and hence is a simple diagnosis.
Infection and foreign body reactions will usually give fat necrosis but overlying dermal involvement and
a suppurative and granulomatous inflammation.
Special stains may be helpful.
Subcutaneous T-cell Lymphoma Alpha Beta type shows a lymphocytic infiltrate in the fat without any sign of
vasculitis, granulomatous inflammation or necrosis. Sometimes a rim of lymphocytes surrounding
individual fat cells is seen and this points to the diagnosis. Submitting tissue for PCR monoclonality is
the best way of diagnosing this condition.
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