Chief Complaint UCSF CME June 24, 2015 27 yo previously healthy - - PowerPoint PPT Presentation

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Chief Complaint UCSF CME June 24, 2015 27 yo previously healthy - - PowerPoint PPT Presentation

6/24/2015 CPS Chief Complaint UCSF CME June 24, 2015 27 yo previously healthy woman is admitted for severe abdominal pain HPI 3 months ago: anorexia, burping, vomiting, and constipation One month later: subjective fevers, night sweats,


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CPS UCSF CME June 24, 2015

Chief Complaint

27 yo previously healthy woman is admitted for severe abdominal pain

HPI

3 months ago: anorexia, burping, vomiting, and constipation One month later: subjective fevers, night sweats, and a pruritic, nodular rash over her R abdomen migrated to R hip

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HPI, continued

Aforementioned symptoms developed while in Peru teaching English and yoga

(Current presentation) Travel to Peru Fever, rash GI symptoms In Peru

HPI, continued

Exposures

Reported intercourse with new male partner (used condom) Swam in dirty water near a zoo in the jungle Camped and trekked through jungle areas Walked barefoot on farms at the yoga center Ate ceviche and raw vegetables

HPI, continued

Sought medical care in Cuzco (2 months before current presentation):

Showed photos of rash to her physician:

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HPI, continued

CBC with eosinophilia (3000), chem panel and LFTs normal Blood cultures + Salmonella typhi Treated with cipro x10 days constitutional symptoms resolved But rash and GI symptoms persisted

HPI, continued

Further w/u for rash and GI sxs (in Cuzco):

Rash biopsy: nonspecific inflammatory changes Stool O+P negative Repeat WBC 14,000 with 44% eos

Treated with ivermectin and triclabendazole (unclear course) Rash, constipation, and crampy abd pain persisted and she returned to the US for further medical care

HPI Cont

Upon return, saw PCP started empiric prednisone 40mg daily for possible allergic or autoimmune process 3 days after starting prednisone, presents to local ED with abrupt worsening of abd pain (current presentation)

Current presentation Travel to Peru Fever, rash GI symptoms In Peru

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Remainder of history

PMH Mild childhood asthma

no intubations no atopic symptoms

G0P0 PSH None NKDA Meds None, except recently

Cipro Ivermectin Triclabendazole Prednisone

Remainder of history

FHx Mother: leukemia Otherwise noncontributory HRB No tob, etoh, illicits, IVDU SHx Lives on San Juan Island with her family Most recently teaching English and yoga in Peru No other travel Exposures as per HPI

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Exam

VS 36.4 78 100/59 20 98% RA Gen: pleasant, WDWN, NAD HEENT: anicteric, EOMI, no conj

  • hemorrhages. OP clear, MMM

Neck: supple CV: RRR, nl S1, S2, no m/r/g Resp: CTAB

Exam, cont

Abd: soft, mild TTP, +rebound, no guarding. No HSM. Hypoactive BS MSK: normal Neuro: A&Ox3, normal Lymph: no supraclavicular or cervical LAD Skin: indurated red/violaceous thick linear rash over R iliac crest. No fluctuance, mild TTP and warmth

Labs

Ca 8.3, Mg 1.6 Albumin 3.0 PT 14.1, PTT 34, INR 1.1

11.3 11.7 279 88 135 3.9 106 21 0.67 11 0.7 46 108 77

Diff: 42% eos

Micro + Imaging

HIV, syphilis, GC/CT, and hepatitis serologies negative Repeat O+P negative x3 Blood cultures pending CT a/p

Inflammation of the ileum and adjacent fluid c/f small perf vs abscess

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Hospital course

Started on ceftriaxone for possible typhoid relapse (and possible perf) Blood cultures neg Multiple serologies pending Abdominal pain improved, was discharged on azithromycin and a dose

  • f albendazole for possible helminthic

infection NOS

Outpatient course

Continues to get new nodules on her abdomen Eos persistently elevated Serologies returned:

High pos filariasis IgG, neg filariasis IgG4 neg strongyloidiasis Ab Neg fasciola Neg toxocara Neg paragonamous

A diagnostic test was received…

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Final diagnosis?

  • A. Typhoid relapse

B. Filariasis C. Echinococcus

  • D. Gnathostomiasis

E. Strongyloidiasis F. I have no idea – can’t wait for Dr. Hollander’s answer!

T y p h

  • i

d r e l a p s e F i l a r i a s i s E c h i n

  • c
  • c

c u s G n a t h

  • s

t

  • m

i a s i s S t r

  • n

g y l

  • i

d i a s i s I h a v e n

  • i

d e a – c a n ’ t w a . .

5% 41% 15% 22% 5% 12%

Follow-up Email, 1 year later (5/2015)

Hello Thankfully, my rash began to slowly disappear about 2 weeks after taking Albendazole. I got a 6-month and 1-year check-up and my Eosinophilia has disappeared! I am back on track, feeling very healthy, alive and parasite free :) I have some very minor discoloration where the rash was and a couple of scars from the Peruvian biopsies, but that's it! Thank you again so much for your expertise, persistence, and incredible support! I don't know what I would have done without you. Regards,

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Final diagnosis

Gnathostomiasis

Special Acknowledgement

  • Dr. Seth Cohen

– Previous UCSF chief resident, 2012-2013 – Current chief fellow, infectious diseases, UWMC

Map of countries with reported acquisition of gnathostomiasis.

Herman J S , and Chiodini P L Clin. Microbiol. Rev. 2009;22:484-492

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Gnathostomiasis

Caused by nematode Gnathostoma spinigerum Acquired by eating uncooked food, esp fish (eg ceviche!)

Gnathostomiasis

Adult worm lives inside gastric wall of definitive host and expels eggs into GI tract 1st stage larva hatch in the presence of water and are then ingested by intermediate hosts, (small crustaceans) where they mature Ingested by second intermediate hosts (fish, frogs, snakes, chickens, pigs), migrate and mature into 3rd stage larva ready to infect humans Most commonly acquired by consumption of undercooked fish (esp tilapia), poultry or pork

Also acquired via penetration of the skin or prenatal transmission Rusnak, CID, 1993

Gnathostomiasis: Clinical

2 forms of disease, visceral and cutaneous

Cutaneous form: Intermittent migratory skin and subcutaneous swellings, eosinophilia CNS involvement (eosinophilic meningitis)

Symptoms occur ~24-48hrs after ingestion with non-specific sx: malaise, fever, urticaria Migrate through subcutaneous tissue migratory swellings for up to 10-12 years!

Rusnak, CID, 1993

Diagnosis: Western blot, performed in Thailand

Thought to be sensitive and specific for this disease

One study examined a case series from 2000-2001

  • f 16 patients in a Thai hospital

Median time from symptoms to diagnosis was 12 months Eosinohilia present in 7 patients Treatment: albendazole 400mg BID x 21 days

Moore, EID, 2003