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Panniculitis

»What is panniculitis?
»Name the various types of panniculitis. How are they classified?
»What is erythema nodosum?
»What is the pathogenesis of erythema nodosum?
»List some of the common underlying conditions associated with erythema nodosum.
»How should a biopsy of erythema nodosum be obtained?
»What are the characteristic microscopic features of erythema nodosum?
»How is erythema nodosum treated?
»What is nodular vasculitis?
»What causes nodular vasculitis?
»Describe the microscopic features of nodular vasculitis.
»What is the differential diagnosis of nodular vasculitis?
»How should nodular vasculitis be treated?
»What are the clinical features of lupus panniculitis?
»Describe the microscopic features of lupus panniculitis.
»What is the significance of diagnosing lupus panniculitis?
»Are sclerema neonatorum and subcutaneous fat necrosis of the newborn the same thing?
»How similar are the microscopic features of sclerema neonatorum and subcutaneous fat necrosis of the newborn?
»Why do these disorders occur in neonates and infants?
»What is pancreatic fat necrosis?
»Are there any characteristic histopathologic features of pancreatic fat necrosis?
»What is the role of a-1 antitrypsin deficiency in the development of panniculitis?
»Name some types of trauma that can produce panniculitis.
»Which infectious organisms can produce panniculitis?
»Describe the role of malignancy in producing panniculitis.
»What is lipodystrophy?
»What is lipoatrophy?
»What is lipohypertrophy?
»Discuss the approach to use when attempting to diagnose an “unknown” case of panniculitis.

 
 
 

What is lipodystrophy?


A, Acquired partial lipodystrophy with associated C3 nephritic factor. Note the prominent wasting of the facial fat in this patient. B, Localized lipoatrophy associated with injection of medication. (Courtesy of Kenneth E. Greer, MD.)
Fig. 19.11 A, Acquired partial lipodystrophy with associated C3 nephritic factor. Note the prominent wasting of the facial fat in this patient. B, Localized lipoatrophy associated with injection of medication. (Courtesy of Kenneth E. Greer, MD.)
Lipodystrophy generally refers to a paucity or complete absence of subcutaneous fat, sometimes due to redistribution. It can be generalized or localized, inherited or acquired. Lipodystrophy can be idiopathic, but is often associated with inherited syndromes, endocrine abnormalities such as insulinresistant diabetes mellitus, complement abnormalities (Fig. 19-11A), or autoimmune disease. It is well recognized that highly active antiretroviral therapy (highly active antiretroviral therapy [HAART], particularly protease inhibitors) causes a distinctive redistribution of subcutaneous fat with accumulation of fat in abdominal and cervical areas and wasting of the face and extremities.

Koutkia P, Grinspoon S: HIV-associated lipodystrophy: pathogenesis, prognosis, treatment, and controversies, Annu Rev Med 55: 303–317, 2004.