1 / 22

Is it really rheumatological ?

Is it really rheumatological ?. S Gupta Rheumatology Study Day 10 th May 2011. Background. 16 years old female. In the UK for the last 4 years Originally from the Congo. 1 of 8 siblings Currently living with 2 older sisters. Both parents deceased. Presentation.

jeslyn
Download Presentation

Is it really rheumatological ?

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Is it really rheumatological ? S Gupta Rheumatology Study Day 10th May 2011

  2. Background • 16 years old female. • In the UK for the last 4 years • Originally from the Congo. • 1 of 8 siblings • Currently living with 2 older sisters. • Both parents deceased.

  3. Presentation • To the Ophthalmologists • 2 /52 h/o reduced vision in right eye. • Non specific findings • But bloods done inc ACE levels and ESR • Seen 2/52 later in Eye clinic again • Vision further reduced to only 1/60. • Other eye normal

  4. Other features • Under dermatologist for 2 years for skin rash • Skin biopsy- s/o inflammatory cells- 1 yr ago. • Massive cervical and axillary lymphadenopathy • Low grade pyrexia last 2 weeks

  5. Rheumatology • Referral to us with ?sarcoidosis ( ACE 127) Further History • H/o SOB during exercise elicited and low grade fever • No joint symptoms • No mouth ulcers • No H/o photosensitivity • H/o Headaches for last 3 weeks • No H/o night sweats

  6. Sarcoidosis • Multisystem inflammatory disease • Lungs + intrathoracic LNs • Non caseating granulomas. • Incidence and prevalence much higher for African Americans • Ocular ass with uveitis • 60% ass with high ACE at diagnosis

  7. Differential Diagnosis • Sarcoidosis • Malignancy • HIV/ TB- though denied any H/o contacts • Sickle cell anaemia- unusual presentation at 16 • Optic Neuritis

  8. Investigations • ACE Level- 127 • ESR- 25 • Hb- 8.7, Hypochromic microcytic anaemia s/o- iron deficiency • MRI brain- suggestive of orbital apex syndrome • HRCT of the chest as a screening for raised ACE levels • Lymph node biopsy

  9. MRI report • Ptosis  of  the  right  eye  with  slight  signal  change  and enhancement  in  the  right  optic  nerve.  The  extra-ocular muscles  close  to  the  orbital  apex  also  show  enhancement  butthe  anterior  portions  show  relatively  normal  appearance.There  is  no  mass  lesion.  The  appearance  would  be  most  inkeeping  with  an  inflammatory  condition.  Multiple  enlarged lymph  nodes  are  seen  in  the  neck.

  10. Further tests • Immunology tests- all negative except ACE levels • Ferritin and TIBC • Quantiferon • Mantoux • Blood film and sickle cell screen • Lumbar Puncture- negative ( by neurologist) • Virology screen- negative.

  11. HRCT of chest

  12. HRCT Report • Bilateral  hilar  and  subcarinal  lymphadenopathy  withcalcifications.  There  are  multiple  scattered  nodules  in  bothlungs  and  also  pleural  based  nodules  and  nodule  within  the oblique  fissure.  In  the  left  lower  lobe  there  isbronchiectasis  with  focal  pleural  thickening  and  linear scarring  which  appears  longstanding.Overall  appearance  is  consistent  with  granulomatous  disease.

  13. Progress • Reviewed repeatedly by Ophthal • Worsening vision, down to only PL • Though Diagnosis not confirmed- • Decision to start iv MethylPred over 3 days

  14. In view of HRCT • Discussion with Resp Consultant • Plan to start Anti TB treatment as on iv Methylpred • Rapid improvement in vision within 36 hours

  15. Positive Mantoux

  16. Diagnosis • Mantoux 30 mm, large blister • Positive Quantiferon. HIV negative • Lymph node- caseating granuloma • Rapid improvement following AKT

  17. An orbital apex syndrome (OAS) has been described as • a syndrome involving damage to the oculomotor nerve (III), trochlear nerve (IV), abducens nerve (VI), • ophthalmic branch of the trigeminal nerve (V1) in • association with optic nerve dysfunction • Visual loss and ophthalmoplegia are often the initial manifestations

  18. Orbital apex syndromes may be caused by • Inflammatory- Sarcoidosis lupus Churg–Strauss syndrome Wegener granulomatosis etc • infectious- Fungi: Aspergillosis, Mucormycosis Bacteria: Streptococcus spp., Staphylococcus spp., Actinomycesspp., Gram-negative bacilli, anaerobes, Mycobacterium tuberculosis, Spirochetes: Treponema pallidum Viruses: Herpes zoster • neoplastic • iatrogenic/traumatic • Vascular processes- sickle cell anaemia

  19. Active histoplasmosis Amyloidosis Asbestosis Berylliosis Diabetes Emphysema Gaucher's disease Hepatitis Hodgkin’s disease Hyperthyroidism Idiopathic pulmonary fibrosis Leprosy Lung cancer Nephrotic syndrome Primary Biliary cirrhosis Pulmonary embolism Scleroderma Silicosis Tuberculosis Increased ACE levels may be a sign of sarcoidosis but also seen in several other disorders

  20. References • Orbital apex syndrome, Steven Yeh and Rod Foroozan, (Neuro-ophthalmology) • National library of Medicine and National Institutes of Health, USA

More Related