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lymphomatoid granulomatosis/fatigue
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[Lymphomatoid granulomatosis--remission induction with interferon-alpha 2b].
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METHODS
A 72-year-old woman was admitted to hospital because of nonproductive cough, acrodistal sensorimotor axonal polyneuropathy, fatigue and 10 kg weight loss over the preceding 9 months.
METHODS
Chest radiogram showed multiple round foci in both lungs. No organs other than the lungs and the
Migratory nodules in the lung: lymphomatoid granulomatosis.
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A 45-year-old woman was admitted with complaints of non-productive cough, chest pain, fatigue and weight loss in the last 4 months. On physical examination moderate hepatosplenomegaly and crackles most notably on the basal region of the right lung were evident. Serial chest X-rays and computed
Unsuspected lymphomatoid granulomatosis in a patient with antisynthetase syndrome.
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Clinical diagnosis of lymphomatoid granulomatosis (LYG) often is difficult, especially in patients with multiple comorbidities. We present a 60-year-old woman with worsening fatigue, night sweats, unintentional weight loss, and dyspnea of 2 weeks' duration. Her medical history was remarkable for
Fatal lymphomatoid granulomatosis with primary CNS-involvement in an immunocompetent 80-year-old woman.
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An 80-year-old woman presented with weight loss, fatigue, dizziness and a brain stem lesion. Extensive work-up revealed lymphomatoid granulomatosis (LYG) with primary clinical manifestation in the central nervous system (CNS), a rare Epstein-Barr virus-driven multisystem lymphoproliferative
An atypical case of a pulmonary mass in an immunocompromised patient.
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Objectives Pulmonary lymphomatoid granulomatosis (PLG) is a rare angiocentric and angiodestructive EBV-associated lymphoproliferative disorder which almost always affects the lungs. PLG is more commonly diagnosed in patients with immunodeficiency and is associated with Epstein-Barr virus
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