Loading...
 
Mediterr J Rheumatol 2019;30(3):190-3
Α 40-Year-Old Woman with Asymmetric Arthritis and Skin Lesions
Authors Information
1Patras University Hospital, Department of Internal Medicine, Division of Rheumatology, Rion, Patras, Greece
2University of Patras Medical School, Rion, Patras, Greece
Full Text

INTRODUCTION

The combination of arthritis and skin lesions represent a usual presentation in our daily clinical practice. Fever can also be an accompanying symptom.In such cases, differential diagnosis includes connective tissue diseases,2 infections, endocrine,3 hematologic4 and malignant diseases5

 

CASE PRESENTATION

A 40-year-old woman was evaluated in our rheumatologic clinic because of joint pain in the lower extremities during the last week.  She mentioned that 3 months ago, she had visited the emergency department of our hospital because of joint pain in the right heel and ankle. She was prescribed NSAIDs with total remission of her symptoms.

On physical examination synovitis of ankles, right knee, right 1st metatarsophalangeal joint and right elbow was seen.  She was prescribed naproxen for 2 weeks.  One week later she was admitted to the hospital because of persisting arthritis of the legs and feet and Achilles tendonitis of both feet. In addition, purple, bullous and painful lesions at the dorsal surface of both feet had appeared recently (Figure 1).

A laboratory work-up showed an elevated CRP (10 mg/dL, normal < 0.8 mg/dL) and ESR (90 mm/h) and a normochromic, normocytic anaemia (Hb=10.9 g/dL). Testing for autoantibodies, viruses, a vaginal and cervical smear, cultures of blood and skin lesion exudates were all negative, as was a purified protein derivative (PPD) skin test.

The patient was thoroughly investigated to rule out infections and malignancies. Computed tomographies of chest and abdomen, as well as the echocardiogram, were normal. Mammography and the ultrasound test of breasts revealed incidentally a fibroadenoma of the left breast.  Biopsy of the skin lesions could not be performed because of their position and possible damage of the underlying tendons.

Although she was treated with wide spectrum antibiotics (even against gonorrhoea), her arthritis and skin lesions were aggravated.

We examined the patient and taking into account the asymmetric arthritis, the pyoderma gangrenosum lesions of the feet and the radiological image of enthesitis of both heel bones (Figure 2), our working diagnosis was a seronegative spondylarthritis.  Therefore, we suggested she should undergo a colonoscopy, even though the patient declined having bowel symptoms.  Meanwhile, we increased the steroids dosage she was receiving from 16 mg of methylprednisolone p.o. daily to 40 mg of methylprednisolone IV.

Colonoscopy was performed and settled the diagnosis of florid Crohn’s Disease.  Treatment with anti-TNF-α agent infliximab (5mg/kg) was initiated and 1 month after the first infusion her arthritis and pyoderma gangrenosum lesions were significantly improved as were the patient’s laboratory tests after a couple of months. (Figure 3 and Figure 4).


Figure 1. Painful nodules of the feet and right ankle.
 




Figure 2. X-rays of the feet during hospital admission showing enthesitis (blue arrows) on both calcanei (film B and C). In contrast, 3 months before she referred to our clinic there is no sign of enthesis involvement (film A).
 




Figure 3. Skin lesions greatly improved after two infusions of Infliximab.
 




Figure 4. Great improvement of complete blood count and acute phase reactants of the patient a couple of months after treatment with Infliximab.
 



DISCUSSION

 

We describe herein a patient with Crohn’s disease (CD) with preceding arthritis and pyoderma gangrenosum, without any intestinal manifestations.  CD is an inflammatory bowel disease (IBD), which includes extraintestinal manifestations (EIM)6 that may or may not  be of parallel clinical activity with the bowel disease.7  These EIM include manifestations from the musculoskeletal system,8,9 skin lesions,10,11 aphthous ulcers and eye involvement (uveitis).The arthritis accompanying CD is usually an asymmetric oligoarthritis affecting mainly large joints with preferential order to knees, ankles, wrists and shoulders.
In addition, a symmetric / asymmetric polyarthritis can be presented, affecting small joints independently of IBD presentation and activity.6,8,13

Skin lesions of CD include erythema nodosum and pyoderma gangrenosum (PG).6,14 It appears that PG has a tendency to appear in females (up to 30% of female patients) and mostly in the lower limbs. It is usually ulcerative when in context of seronegative spondyloarthropathies,9 but other types have also been observed, such as nodular, pustular, bullous, or vegetative10 in other diseases, too.  It has been reported that one quarter of patients with IBD may present with extraintestinal manifestations preceding even 5 months -on average- prior to IBD diagnosis.6,7 However, it was surprisingly noted that peripheral arthritis along with PG in particular, do not precede IBD diagnosis as this occurred in our patient.7

Anti-TNF-α blockers have been approved for CD management.17,18 Furthermore, studies have shown remarkable results in treating the EIM; TNF-α blockers are equally satisfactory in both the musculoskeletal manifestations  (peripheral arthritis, axial arthropathy) and skin lesions (erythema nodosum and PG).  Our patient had an IBD preceded by an asymmetric arthritis resistant to common/usual therapeutic manipulations (including high doses of steroids) and PG lesions manifested as an unusual (bullous) form that eventually progressed to the ulcerative type.  Anti-TNF-α therapy improved the patient’s disease remarkably and quickly, immediately following the first i.v. infusion.

In conclusion, the diagnostic approach and management of patients with arthritis and skin lesions can be challenging. A detailed history, a thorough clinical examination and relevant problem-oriented tests and a careful follow-up can help us establish the proper diagnosis and treatment.


CONFLICT OF INTEREST

The authors declare no conflict of interest.

References
  1. Bachmeyer C, Vigouroux A, Moguelet P. Fever, arthritis, and cutaneous lesions. Eur J Intern Med 2017;Dec;46:e3-e4. [https://doi.org/10.1016/j.ejim.2017.04.023] [PMID: 28483370]
  2. Jacques T, Sudoł-Szopińska I, Larkman N, O’Connor P, Cotten A. Musculoskeletal Manifestations of Non-RA Connective Tissue Diseases: Scleroderma, Systemic Lupus Erythematosus, Still’s Disease, Dermatomyositis/Polymyositis, Sjögren’s Syndrome, and Mixed Connective Tissue Disease. Semin Musculoskelet Radiol 2018;Apr;22(2):166-79. [https://doi.org/10.1055/s-0038-1639473] [PMID: 29672805]
  3. Boswell SB, Patel DB, White EA, Gottsegen CJ, Forrester DM, Masih S, et al. Musculoskeletal manifestations of endocrine disorders. Clinical Imaging 2014;Jul-Aug;38(4):384-96. [https://doi.org/10.1016/j.clinimag.2014.02.014] [PMID: 24642251]
  4. Morais SA, du Preez HE, Akhtar MR, Cross S, Isenberg DA. Musculoskeletal complications of haematological disease. Rheumatology (Oxford) 2016; Jun;55(6):968-81. [https://doi.org/10.1093/rheumatology/kev360] [PMID: 26443208]
  5. Wen J, Ouyang H, Yang R, Bo L, Zhang Y, Tang M, et al. Malignancy dominated with rheumatic manifestations: A retrospective single-center analysis. Sci Rep 2018;8, Article 1786. [https://doi.org/10.1038/s41598-018-20167-w]
  6. Chen JH, Li CJ, Zhi M. Extraintestinal manifestations of inflammatory bowel disease. World Chinese J Dig 2016. [https://doi.org/10.11569/wcjd.v24.i1.1]
  7. Vavricka SR, Rogler G, Gantenbein C, Spoerri M, Vavricka MP, Navarini AA, et al. Chronological order of appearance of extraintestinal manifestations relative to the time of IBD diagnosis in the Swiss Inflammatory Bowel Disease Cohort. Inflamm Bowel Dis 2015;2015 Aug;21(8):1794-800. [https://doi.org/10.1097/MIB.0000000000000429] [PMID: 26020601]
  8. Atzeni F, Defendenti C, Ditto MC, Batticciotto A, Ventura D, Antivalle M, et al. Rheumatic manifestations in inflammatory bowel disease. Autoimmun Rev 2014;Jan;13(1):20-3. [https://doi.org/10.1016/j.autrev.2013.06.006] [PMID: 23774109]
  9. Ye MJ, Ye JM. Pyoderma gangrenosum: A review of clinical features and outcomes of 23 cases requiring inpatient management. Dermatol Res Pract 2014;2014:461467. [https://doi.org/10.1155/2014/461467] [PMID: 25374597] [PMCID: PMC4206920]
  10. Suvirya S, Pathania S, Singhai A. A case of bullous pyoderma gangrenosum. BMJ Case Rep 2019;Mar 31;12(3):pii: e228772. [https://doi.org/10.1136/bcr-2018-228772] [PMID: 30936355]
  11. Roth N, Biedermann L, Fournier N, Butter M, Vavricka SR, Navarini AA, et al. Occurrence of skin manifestations in patients of the Swiss Inflammatory Bowel Disease Cohort Study. PLoS One 2019; 14(1):e0210436. [https://doi.org/10.1371/journal.pone.0210436] [PMID: 30682031] [PMCID: PMC6347222]
  12. Atzeni F, Defendenti C, Ditto MC, Batticciotto A, Ventura D, Antivalle M, et al. Rheumatic manifestations in inflammatory bowel disease. Autoimmun Rev 2014 Jan;13(1):20-3. [https://doi.org/10.1016/j.autrev.2013.06.006] [PMID: 23774109]
  13. Hiller A, Biedermann L, Fournier N, Butter M, Vavricka SR, Ciurea A, et al. The appearance of joint manifestations in the Swiss inflammatory bowel disease cohort. PLoS One 2019;14(4):e0211554. [https://doi.org/10.1371/journal.pone.0211554] [PMID: 31039159] [PMCID: PMC6490952]
  14. Gameiro A, Pereira N, Cardoso JC, Gonçalo M. Pyoderma gangrenosum: Challenges and solutions. Clin Cosmet Investig Dermatol 2015 May 28;8:285-93. [https://doi.org/10.2147/CCID.S61202] [PMID: 26060412] [PMCID: PMC4454198]  
  15. Ye MJ, Ye JM. Pyoderma gangrenosum: A review of clinical features and outcomes of 23 cases requiring inpatient management. Dermatol Res Pract 2014;2014:461467. [https://doi.org/10.1155/2014/461467] [PMID: 25374597] [PMCID: PMC4206920]
  16. Suvirya S, Pathania S, Singhai A. A case of bullous pyoderma gangrenosum. BMJ Case Reports 2019;12(3). pii: e228772. [https://doi.org/10.1136/bcr-2018-228772] [PMID: 30936355]
  17. Lakatos PL, Lakatos L, Kiss LS, Peyrin-Biroulet L, Schoepfer A, Vavricka S. Treatment of extraintestinal manifestations in inflammatory bowel disease. Digestion 2012;86 Suppl 1:28-35. [https://doi.org/10.1159/000341950] [PMID: 23051724]
  18. Vavricka S, Scharl M, Gubler M, Rogler G. Biologics for Extraintestinal Manifestations of IBD. Curr Drug Targets 2014;15(11):1064-73. [https://doi.org/10.2174/1389450115666140908125453] [PMID: 25198785]