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“We present a case of Loa loa infection in a patient, 21 years after visiting an endemic area for only 4 days. To our knowledge, this case represents the longest time for the diagnosis of loiasis H 89 manufacturer to be made post-exposure in a traveler and emphasizes that even short exposures can place travelers at risk. A 60-year-old man was referred to one of the authors (M. B.) after his dermatologist

(J. K. G.) extracted a filamentous round worm from a right upper eyelid swelling (Figure 1). The patient had been experiencing migratory facial edema for the past 2 years. He had visited various physicians during that time period to evaluate transient swellings on the side of his nose, left eyebrow, and right cheek. INK 128 clinical trial Workup included a CT scan of the orbits, and an MRI brain—both of which were unrevealing except for a right lacrimal gland swelling on the MRI reported as “suspicious for lymphoma.” Three biopsies were performed prior to consultation, and no evidence of lymphoma or granulomatous disease was identified. The patient was told that these swellings could be a reaction to the facial surgery he had prior to becoming symptomatic. The medical history was significant for hypertension, Gleason 6 prostate cancer, and a rhytidectomy (face lift) 10 years ago. Medications included an aspirin (81 mg) and olmesartan–hydrochlorothiazide.

Social history was negative for alcohol abuse or tobacco. Although the patient had an extensive travel history throughout Europe, Asia, and South America,

the case is notable in that he had only visited sub-Saharan Africa once: In 1989, he traveled to Lagos, Nigeria for a 3-day business trip. He did not recall any unusual bites at that time and was in an urban setting at all times during the travel. The physical examination was unremarkable for further tissue swellings. In addition, there were no stigmata of chronic lymphedema or organomegaly. The rest of the examination was normal. The white blood cell count was 7,200 cells/microliter with Fossariinae 210 absolute eosinophils. Testing for peripheral blood microfilariae was negative. The IgE level was within the normal reference range, and the urinalysis was unremarkable. Serologies were not performed since we were able to send the worm for a definitive PCR diagnosis. Chest X-ray revealed pleural plaques and rounded multifocal opacities that were deemed on PET scan to be the sequelae of prior asbestos exposure. Review of formalin-fixed, paraffin-embedded tissue sections from multiple biopsies from the patient’s neck, right inner cheek, forehead, and right eyelid between March 2009 and May 2010 demonstrated patchy lymphocytic infiltrates, sometimes extending into the subcutaneous fat with occasional multinucleated giant cells and areas of necrosis. No prominent eosinophilic infiltrates were seen on any of the biopsies. A white roundworm measuring approximately 6.5 cm in length and 0.