Indian Dermatology Online Journal

LETTER TO THE EDITOR
Year
: 2017  |  Volume : 8  |  Issue : 4  |  Page : 294--296

The whiplash rash


Ajay M Brahmnalkar1, Balkrishna P Nikam2, Harsimran Kaur2,  
1 Department of Medicine, Krishna Institute of Medical Sciences, Karad, Maharashtra, India
2 Department of Dermatology, Krishna Institute of Medical Sciences, Karad, Maharashtra, India

Correspondence Address:
Balkrishna P Nikam
Department of Dermatology, Krishna Institute of Medical Sciences, Karad, Maharashtra
India




How to cite this article:
Brahmnalkar AM, Nikam BP, Kaur H. The whiplash rash.Indian Dermatol Online J 2017;8:294-296


How to cite this URL:
Brahmnalkar AM, Nikam BP, Kaur H. The whiplash rash. Indian Dermatol Online J [serial online] 2017 [cited 2021 Jun 25 ];8:294-296
Available from: https://www.idoj.in/text.asp?2017/8/4/294/209623


Full Text

Sir,

A 16-year-old female presented with high grade fever, associated with evening spike, persistent itchy lesions on body, and acute pain in shoulder, knee, and ankle joints for 3 weeks. She was hospitalized to evaluate the cause of her fever and polyarthralgia. Dermatological examination revealed reddish brown and violaceous patches with few scaly or crusted lichenoid papules and plaques widely distributed on the abdomen, back [Figure 1] and [Figure 2], and proximal upper extremities. Lesions were intensely pruritic and appeared flagellate or bizarre due to scratching. Hair, nails, and mucous membranes were normal. She was also found to have cervical lymphadenopathy and a moderate grade splenomegaly. Routine investigations were suggestive of anemia, leukocytosis, a raised erythrocyte sedimentation rate (ESR), a deranged hepatic profile and a very high serum ferritin level (>4000μg/l). A detailed fever profile was done to rule out any infectious cause. Her anti-nuclear antibody (ANA) and Rheumatoid arthritis factor (RF) were negative. Histopathological examination [Figure 3] revealed focal vacuolization, multiple discrete necrotic epidermal keratinocytes, and a mixed superficial perivascular dermal infiltrate. Characteristic lichenoid pruritic bizarre rash, clinical, laboratory findings, and histopathology assisted in establishing the diagnosis of Adult Onset Still's Disease (AOSD).{Figure 1}{Figure 2}{Figure 3}

When features of juvenile rheumatoid arthritis (JRA) syndrome appear in adults, it is referred to as AOSD, as coined by Bywaters.[1] It is a systemic inflammatory disorder characterized by high fever, arthralgia, rash, and variable systemic features. Cases of AOSD are diagnosed based on Yamaguchi and Ohta criteria,[2] which include high intermittent fever, arthralgia, typical rash and leukocytosis as the major ones whereas sore throat, lymphadenopathy and/or splenomegaly, liver dysfunction, negative ANA, and RA factor constitute the minor criteria. Five or more criteria including two major ones should be present to make the definitive diagnosis. Serum ferritin levels, as in our case, are much higher in AOSD and hemophagocytic syndrome as compared to other autoimmune or inflammatory disorders. A dermatologist must consider AOSD in a febrile illness with rash if the serum ferritin is >1000μg/l.[3]

Though known for its classic, salmon-pink, evanescent rash, recent literature on AOSD describes more of atypical eruptions; approximately 29–78% cases are commonly referred to as “persistent pruritic eruptions”.[4] They may be urticarial, lichenoid, dermographism-like, dermatomyosistis-like, prurigo pigmentosa-like or lichen amyloidosis-like. Rarely reported are acneiform, eczematoid, peau'd orange-like or vesicopustular eruptions.[1]

In many cases, rash and fever occur for months or even years before joint symptoms develop. Further, the atypical cutaneous features are reported more often than the classic ones. Dermatologists play a pivotal role in the early diagnosis of such cases and their delineation from other causes of flagellate dermatoses. Causes such as Shiitake mushroom poisoning, chemotherapy (Bleomycin or Docetaxel) induced whiplash rash, dermatomyositis and dermatitis artefacta were ruled out on the basis of clinical history and histopathological examination.[5] Persistent linear pigmentation and dermatomyositis-like flagellate eruption as in our case has been associated with poor prognosis and severe clinical outcomes.[6] Hence, such rash in a case of AOSD should alert the clinician for immediate and aggressive systemic management.

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Conflicts of interest

There are no conflicts of interest.

References

1Lee JB, Kim JW, Lee SS, Kim SJ, Won YH, Lee SC. Adult-onset Still's disease with vesiculopustules on the hands and feet. J Korean Med Sci. 2002;17:852-5.
2Ohta A, Yamaguchi M, Kaneoka H, Nagayoshi T, Hiida M. Adult Still's disease: Review of 228 cases from the literature. J Rheumatol 1987;14:1139-46.
3Jandus P, Wang W, Seitz M, Wermelinge F, Kohler H. “High Serum Ferritin in Adult-Onset Still's Disease,” Int J of Clin Med 2010;1:81-3.
4Akkurt ZM, Bozkurt M, Uçmak D, Türkcü G, Uçak H. Atypical cutaneous features in adult onset Still's disease. Indian J Dermatol Venereol Leprol 2014;80:250-3.
5Bhushan P, Manjul P, Baliyan V. Flagellate dermatoses. Indian J Dermatol Venereol Leprol 2014;80:149-52.
6Ohashi M, Moriya C, Kanoh H, Kinomura Y, Terakura Y, Kasahara S, et al. Adult-onset Still's disease with dermatomyositis-like eruption. J Dermatol 2012;39:958-60.