S10C2-Panniculitides 10

 Septal Panniculitis

Erythema Nodosum

If attention is given solely to histologic features, panniculitides generally are difficult to subclassify. There is some utility in dividing the panniculitides into septal and lobular categories, depending on the distribution of the inflammatory infiltrates. The distinctions, however, are relative; septal lesions may show minor lobular components and lobular lesions commonly have septal components. In the category of lobular patterns, if the infiltrates are prominently lobular, then this component generally should be given primacy, regardless of the character of the septal component. In practice, it seems likely that most of the panniculitides are actually vasculitides of the subcutaneous tissue (even though most of the infiltrates are lymphohistiocytic in character). Physiologic mechanism may influence the expressions of inflammation in subcutaneous fat; in cold weather, blood may be shunted to the lobules away from the dermis. Hot weather may influence the vascular plexus in the opposite manner with increased circulation to the dermis and the septa, and a decrease in the blood flow to the lobules. Similarly, the metabolic activity of adipose tissue may influence the vascularity of the fat and, in turn, influence the distribution of inflammation in response to injury.

Included in the category of septal panniculitides are those disorders generally classified as erythema nodosum. Some lobular disorders, clinically in a distribution that is typical of erythema nodosum, may be nodular, but to include lobular disorders in the septal category would defeat the utility of the histologic category. In spite of the clinical characteristics, these lobular variants are better classified as something other than classic erythema nodosum. It, perhaps, is more appropriate to reserve the classical designations as clinically descriptive terms; at the histologic level, histologic characterizations seem to be preferable.

The early changes of lymphohistiocytic septal panniculitis (erythema nodosum) are characterized by little alteration in the physical dimensions of the affected fibrous septa. Inflammation is mostly perivascular in the septa and lymphohistiocytic in character. A rather characterisitic, but uncommon lesion of early erythema nodosum, is a minute palisaded granuloma. Small histiocytes cluster radially around a small angulated cleft in the inflamed septum; this distinctive lesion is one of Miescher’s granulomas (Meischer described a variety of granulomas) of erythema nodosum (S10,C3,P1-1 & 2).

Better developed lesions of lymphohistiocytic septal panniculitis (erythema nodosum-like) show widening of the septa with fibrosis, edema, fibrin deposits, and perivascular and interstitial infiltrates of lymphocytes and histiocytes. The fibrous tissue and the infiltrates extend from the septa into the neighboring adipose tissue; in this manner, the septa are widened by the process of substitutive fibrosis (newly formed fibrous tissue creeps from the periphery toward the center of affected lobules). Small granulomas and multinucleated giant cells collect in the fibrous septa and, even more prominently, they collect in the newly formed fibrous tissue which extends into the fat. The granulomatous reaction, in part, may be a response to damaged adipose tissue (S10,C3,P1-3 & 4). Old, chronic lesions with both marked septal changes  and prominent granulomatous changes are sometimes characterized as subacute migratory panniculitis.

 

Requena L, Yus ES: Panniculitis. Part 1. Mostly septal panniculitis. J Am Acad Dermatol 2001; 45:163-83.

Tarroch X, et al: Subcutaneous nodules in Whipple’s disease. J Cutan Pathol 2001;28: 368-70.

Lobular Panniculitis

(lipogranulomatous reaction)

In evaluating patterns of lobular inflammation in adipose tissue, the basic reaction of fat to injury must be a consideration. Damaged lipocytes may degenerate but, in the act, may leave behind pools of free lipids. The pools of lipids appear as rounded, empty defects;  they are symmetrically rounded, but vary in size. The lipid material evokes a histiocytic response that may be lipophagic, or frankly granulomatous. In the granulomatous category, a clue to the nature of the granuloma is the presence of symmetrically rounded defects in the center of some of the granulomas. These combined patterns of rounded defects and granulomatous components qualify as a lipogranulomatous response (S10,C4,P2-1-4). In the past, this type of reaction was given recognition as a specific category of lipogranulomatous panniculitis (Rothman and Makai). In some examples of lipogranulomatous reaction, the defects come to be outlined by convoluted membranes (a peculiar reaction of histiocytes to free lipids in the tissue. These variations may include irregular deposits that bulge into the lumens of the defects; the bulges and convolutions may be mistaken for parasites (S10C4aP2a-1-5).

Diffuse, Neutrophilic, Lobular Panniculitis

An uncommon pattern of lobular panniculitis is characterized by diffuse, interstitial (among lipocytes) infiltrates of neutrophils. In contrast to a cellulitis or fasciitis, the infiltrating cells do not tend to break down to produce necrosis and suppuration (S10, C5,P3-1-3). In some examples as a lesion evolves, histiocytes replace the neutrophils as the preponderant component of the interstitial infiltrates (S10C6P4-1-3). Some aspects (suppuration not being one of them) of these reactions might be compared to the interstitial infiltrates of neutrophils that are a basic part of the interstitial reaction in the “leukocytoclastic angiitides,” or Sweet’s syndrome of the dermis. This type of reaction is seen in early lesions in the setting of so-called Weber-Christian disease. In later stages, lipogranulomatous changes (a basic reaction of adipose tissue to injury) may be the chief histologic feature.

Calcifying Panniculitis

A distinctive, lobular panniculitis is occasionally a feature of patients with renal failure who are on dialysis. It is characterized by both septal and lobular alterations. The lobular changes tend to be in the nature of coagulative necrosis with preservation of ghost outlines of lipocytes (increased acidophilia and loss of nuclear staining). Lipocytes degenerate to form lipid-filled cysts; in turn, the cysts evoke an lipogranulomatous response. Small vessels of the lobules contain fibrin thrombi. Calcification of the media of small, muscular vessels is an important feature of the reaction; it is often associated with a delicate, fibrous hyperplasia of the intima and narrowing of the lumen of the affected vessels (S10C5P3-4-8). Calcification of elastic fibers in patterns which resemble the changes of pseudoxanthoma elasticum may also be a feature (S10C5aP3a-1-8). The thrombotic process may involve vessels of the dermis and lead to areas of necrosis and ulceration. The process is associated with abnormal levels of calcium and phosphorus in the blood. I would favor the interpretation that thrombosis of vessels is the primary insult. The calcification of muscular vessels is indicative of an abnormality in the blood level of calcium and phosphorus; it is evidence of a basic affinity of elastica for deposits of calcium.

Walsh J, Fairley JA: Calcifying disorders of the skin. J Am Acad Dermatol 1995;33:693-706.

Granulomatous Lobular Panniculitis

Granulomatous patterns are common in inflammatory processes affecting adipose tissue. Lipogranulomatous reactions are discussed above. Some examples are relatively pure granulomas with little evidence of either necrosis, or non-specific infiltrates of inflammatory cells. For such lesions, if special stains are negative, sarcoidosis should be mentioned in the differential diagnosis. Some examples are associated with non-specific infiltrates of inflammatory cells and are necrotizing and destructive; vasculitic changes may be represented (S10C7P5-1-6). For such examples, special stains are indicated; an infectious process should be ruled out. If stains and cultures (and molecular probes) are negative, such patterns might then suggest the possibility of erythema induratum (another clinical designation of dubious value in histologic classifications), a necrotizing, granulomatous lobular panniculitis.

 

 

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