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Biomedical subjects

Monika Srivastava

Publications and source records attributed to Monika Srivastava.

7 recordsLinked to original sources

Neutrophilic eccrine hidradenitis masquerading as facial cellulitis.

Neutrophilic eccrine hidradenitis typically manifests as erythematous plaques on the face, trunk, or extremities. This eruption has been associated with numerous factors, but most commonly is seen with chemotherapy, particularly cytarabine. We report a 73-year-old woman with acute myelogenous leukemia who developed rapidly expansive neutrophilic eccrine hidradenitis mimicking facial cellulitis only after a course of cytarabine was followed by granulocyte-colony stimulating factor. Prompt diagnosis is imperative to prevent prolonged antimicrobial therapy.

Aged↗

Primary cutaneous nodular amyloidosis in a patient with Sjögren's syndrome.

A 71-year-old woman with a history of Sjögren's syndrome presented for evaluation of a waxy nodule present on the scalp for 6 months. Histopathologic examination revealed deposition of homogenous eosinophilic material throughout the reticular dermis consistent with amyloidosis. Primary cutaneous nodular amyloidosis is a rare phenomenon characterized by the deposition of immunoglobin light chains by a clonal plasma cell population. Patients need to be monitored for progression to systemic amyloidosis or plasma cell dyscrasias.

Aged↗

Carney complex.

A 55-year-old man with a history of two atrial myxomas presented for evaluation and removal of skin lesions. Histopathologic examination showed a well-circumscribed lesion that was consistent with a myxomatous polyp. Carney complex is a syndrome with multiple neoplasias, which is characterized by mucocutaneous myxomas, cardiac myxomas, lentigines, and endocrine abnormalities. Patients with Carney complex need to be monitored for the development of cardiac myxomas and endocrine tumors.

Humans↗

Axillary granular parakeratosis.

A 71-year-old man developed a pruritic axillary eruption. Histopathologic examination showed laminated orthokeratosis, parakeratosis, and hypergranulosis. There changes were consistent with a diagnosis of axillary granular parakeratosis. Axillary granular parakeratosis is an intertriginous eruption that is usually found in the axillae of middle-aged women and is characterized clinically by pruritic, erythematous, hyperkeratotic plaques and histologically by parakeratosis with retention of keratohyaline granules. Pathophysiology is thought to involve a defective profilaggrin-filaggrin pathway. Evidence-based treatment of this disorder is not available.

Aged↗

Drug-induced, Ro/SSA-positive cutaneous lupus erythematosus.

OBJECTIVE: To study the clinical and immunopathologic findings of drug-induced, Ro/SSA-positive cutaneous lupus erythematosus (CLE). DESIGN: Retrospective medical and laboratory record review. SETTING: Immunodermatology Division of Johns Hopkins Hospital (Baltimore, Md). PATIENTS: Of 120 patients found to have anti-Ro/SSA antibodies by hemagglutination and/or double immunodiffusion, 70 had clinical and immunopathologic confirmation of CLE. Fifteen of these 70 patients had a history of new drug exposure, defined as less than 6 months, associated with disease development. RESULTS: The disease-associated drugs included hydrochlorothiazide (5 patients), angiotensin-converting enzyme inhibitors (3 patients), calcium channel blockers (3 patients), interferons (2 patients), and statins (2 patients). The most common presentations were photodistributed diffuse erythema and subacute CLE-type lesions without evidence of significant systemic disease. All specimens revealed interface dermatitis and fine granular IgG deposition along the basement membrane zone and throughout the epidermis. Most patients experienced improvement or resolution of clinical lesions within 8 weeks and decrease of Ro/SSA titers within 8 months after discontinuation of drug treatment. CONCLUSIONS: Antihypertensive drugs are the most commonly associated with Ro-positive CLE. Clinical and immunopathologic features of this drug-induced variant do not seem to differ from the idiopathic disease. In most cases, the disease improves or resolves on discontinuation of the offending drug treatment. It is not known if these drugs precipitate disease in patients who have subclinical disease. Drug-induced Ro/SSA-positive CLE should be included on the differential diagnosis in patients presenting with photosensitive or subacute CLE-type eruptions.

Adult↗

Isolated conjunctival amyloidosis--a case report.

Isolated conjunctival amyloidosis is extremely rare and usually diagnosed histologically instead of clinically. This has been variously reported as an unusual cause of ptosis, complication of trachoma, painless nodular aggregates and recurrent subconjunctival hemorrhages. Once diagnosed, evaluation for systemic disease is advised though results of examination are almost always negative and frustrating.

Amyloidosis↗