scleredema adultorum/edema

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Scleredema adultorum of Buschke presenting as periorbital edema: a diagnostic challenge.

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Scleredema adultorum is a rare sclerotic disorder characterized by diffuse swelling and nonpitting induration of the skin. Its occurrence has been documented in association with infections, diabetes mellitus, paraproteinemia, multiple myeloma, and monoclonal gammopathy. We report an unusual case of

Scleredema: an unusual presentation with edema limited to scalp, upper face, and orbits.

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Scleredema of Buschke with prominent periorbital edema.

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Scleredema adultorum of Buschke with prominent periorbital edema in a Tunisian patient with diabetes mellitus: a case report.

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Scleredema of Buschke in a child with cardiac involvement.

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A few descriptions of scleredema of Bushke associated with cardiac involvement in children have been reported. We report a case of an 11-year-old boy with diffuse nonpitting edema of the trunk and face associated with cardiac involvement.

Scleredema adultorum associated with localized myositis.

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A 70-year-old man presented with large areas of brawny edema of the skin and neck and weakness of the muscles of the forearm. Biopsy revealed scleredema adultorum with inflammatory changes in the forearm muscle. An electromyogram showed a mixed pattern compatible with myositis.

[Buschke's scleredema and carditis: a clinical case].

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An 11-year old girl who presented non-pitting edema of the face and neck, shoulder pain and a gallop rhythm about 10 days after a febrile episode with sore throat is described. The mask-like facial appearance and limited movement of the neck led to suspect scleredema which may be accompanied by

Buschke's scleredema and concomitant diseases: report of five cases and literature review.

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Scleredema adultorum or Buschke's scleredema is a rare disorder that belongs to the group of mucinoses. Diffuse, sudden swelling, hardening and induration of the skin can occur in children and younger women as well as in older men. The dermis is thickened because of the increased collagen

[Systemic Buschke's scleredema with cardiomyopathy, monoclonal IgG kappa gammopathy and amyloidosis. Case report with autopsy].

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A 73 year old retired truck driver and blacksmith was studied in June 1996 for thoracic pain and was diagnosed as acute pericarditis which responded well to steroid treatment. In January 1997, he noted swelling of the abdominal skin, genitalia and limbs, sparing the feet. He was euthyroid, did not

Case of suspected connective tissue disease presenting as chronic edema or swelling of face, neck, and upper trunk.

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An adequate biopsy that includes the subcutaneous tissue is very helpful in the evaluation of patients with suspected connective tissue disease. However, the histologic features must often be correlated with the clinical features and other laboratory tests for a definitive diagnosis. An objective

Therapy-related changes of the bone marrow in chronic idiopathic myelofibrosis.

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In chronic myeloproliferative disorders (CMPDs) a conflict of opinion exists regarding therapy-induced bone marrow (BM) changes and the evolution of myelofibrosis during the lengthy course of the disease. For a more elaborate study of these features chronic idiopathic myelofibrosis (IMF) seems to be

Hyaluronidase in Dermatology: Uses Beyond Hyaluronic Acid Fillers

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Hyaluronidase is mostly widely recognized for its off-label use in correction of complications of hyaluronic acid fillers. However, its utility in other aspects of dermatology is less widely acknowledged. We describe the varied uses of hyaluronidase in dermatology and the underlying evidence base

Sclerema neonatorum: a review of nomenclature, clinical presentation, histological features, differential diagnoses and management.

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OBJECTIVE To review published literature on sclerema neonatorum (SN) in order to clarify its clinical presentation, histological features and management compared with two other diseases: subcutaneous fat necrosis of the newborn (SCFN) and scleredema. METHODS PubMed database was searched using the

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