The second part of our review of panniculitis summarizes the clinicopatholo
gic features of the mostly lobular panniculitides. Erythema induratum of Ba
zin (nodular vasculitis) represents the most common variant of lobular pann
iculitis with vasculitis, although controversy persists about the nature of
the involved vessels. Mostly lobular panniculitides without vasculitis com
prise a series of disparate disorders. These include sclerosing panniculiti
s that results from chronic venous insufficiency of the lower extremities;
panniculitis with calcification of the vessel walls such as calciphylaxis a
nd oxalosis; and inflammatory diseases with crystals within the adipocytes
such as sclerema neonatorum, subcutaneous fat necrosis of the newborn, and
poststeroid panniculitis. Connective tissue diseases, such as systemic lupu
s erythematosus and dermatomyositis, pancreatic diseases, and alpha (1)-a n
titrypsin deficiency may also show a mostly lobular panniculitis with chara
cteristic histopathologic features. Lobular panniculitis may also be an exp
ression of infections, trauma, or factitial causes involving the subcutaneo
us fat. Lipoatrophy refers to a loss of subcutaneous fat due to a previous
inflammatory process involving the subcutis, and it may be the late-stage l
esion of several types of panniculitis. In contrast, lipodystrophy means an
absence of subcutaneous fat with no evidence of inflammation and often the
process is associated with endocrinologic, metabolic, or autoimmune diseas
es. Finally, cytophagic histiocytic panniculitis is the term that has been
used to describe two different processes: one is inflammatory, a lobular pa
nniculitis, and the other one is neoplastic, a subcutaneous T-cell lymphoma
. The only common feature of these two different processes is the presence
of cytophagocytosis in the lesions.