Is it really an erysipelas?
Journal of Microbiology and Infectious Diseases /
JMID
2014; 4 (4): 168-169
doi: 10.5799/ahinjs.02.2014.04.0163
CLINICAL IMAGE
Is it really an erysipelas?
Muhammed Bekçibaşı1, İlker İnanç Balkan2, Ayşe Salihoğlu3, Ali Mert4
Dicle University School of Medicine,Department of Infectious Diseases and Clinical Microbiology, Diyarbakır, Turkey
İstanbul University Cerrahpaşa School of Medicine,Dept. of Infectious Diseases and Clinical Microbiology, İstanbul, Turkey
3
İstanbul University Cerrahpaşa School of Medicine,Department of Hematology, İstanbul, Turkey
4
İstanbul Medipol University School of Medicine,Department of Internal Medicine, İstanbul, Turkey
1
2
ABSTRACT
Primary cutaneous anaplastic large cell lymphoma is characterized by red-brown plaques or nodules on the skin, may
mimic skin and soft tissue infections and is usually related with high mortality. A case that was followed up as complicated erysipelas due to similar clinical findings but diagnosed as primary cutaneous anaplastic large cell lymphoma with
histopathological examination has been presented in this report. J Microbiol Infect Dis 2014; 4(4): 168-169
Key words: Erysipelas, diffuse anaplastic large cell lymphoma, fever
Bu gerçekten bir erizipel mi?
ÖZET
Primer kutanöz anaplastik büyük hücreli lenfoma, deride kırmızı-kahverengi plaklar veya nodüllerle karakterize olup
deri-yumuşak doku enfeksiyonlarını taklit edebilmekte ve genellikle yüksek oranda mortaliteyle seyretmektedir. Bu yazıda benzeşen klinik bulguları nedeniyle komplike erizipel ön tanısıyla izlenen ancak histopatolojik inceleme ile primer
kutanöz anaplastik büyük hücreli lenfoma tanısı konulan bir olgu sunulmuştur.
Anahtar kelimeler: Erizipel, diffüz anaplastik büyük hücreli lenfoma, ateş
CASE
A 28 year old female patient was admitted with diffuse erythema, edema and pain on the right thigh
emerging six weeks ago and spreading bi-directionally towards the genital and popliteal areas. She
described fever for 6 weeks. No trauma or any invasive procedure to the right thigh was defined. She
was under immunosuppressive treatment (prednisolone 8-16 mg/day + methotrexate 10 mg/week) for
six months due to rheumatoid arthritis. Various antibacterial agents (amoxicillin-clavulanate, ampicillinsulbactam, meropenem, daptomycin, vancomycin)
were used for a total duration of 5 weeks in different
centers with diagnosis of complicated cellulitis, but
she did not respond to any treatment.
In physical examination; the cachectic and exhausted appearance of the patient was remarkable.
Her fever was 38.6°Ϲ, arterial pressure 90/60 mm/
Hg, respiratory rate 28 /min and heart rate 96 beats/
min. Respiratory sounds were decreased to an inaudible level on the bases of both lungs.
The erythematous, indurated soft tissue lesion
(Figure 1) on the right thigh had a shiny dark-red
appearance and a sharp demarcation line and there
were satellite nodular indurations on the knee. No
abscess formation was detected sonographically in
subcutaneous deep tissues.
In the laboratory examination; Hgb 8 g/dl, WBC
12,700/mm3, platelets 60,000/mm3, MCV: 96 fL,
ESR 6 mm/h, CRP 101 mg/ L, Creatinine 0.4 mg/
dl, ALT 10 U/L, AST 66 U/L, Total bilirubine 1.2, and
INR 1.4. Arterial blood gas analysis; pO2: 71 mmHg,
pCO2: 20 mmHg, Lactate: 6 mEq/L. Chest X-Ray
revealed bilateral pleural effusion.
In the first hours of admittance, the general
medical condition of the patient deteriorated and
she was transferred to intensive care unit with noninvasive mechanical ventilation support. Because
Correspondence: Muhammed Bekçibaşı, Dicle University School of Medicine, Department of Infectious Diseases and
Clinical Microbiology, Diyarbakır, Turkey Email:
Received: 06 February 2014, Accepted: 08 April 2014
Copyright © Journal of Microbiology and Infectious Diseases 2014, All rights reserved
Bekçibaşı M, et al. Is it really an erysipelas?
the clinical picture was compatible with SIRS (Systemic Immune Response Syndrome), imipenem 2
g/day IV + linezolid 1200 mg/day IV was initiated
empirically after obtaining blood cultures. Punch biopsy was conducted from the lesion. No bacterial
growth was detected in the pleural fluid sample and
cytological assessment yielded no pathology.
169
clophosphamide, adriamycin, vincristine, prednisolone) was initiated. On the fifth day of chemotherapy, the patient became dyspnea and acute signs of
disseminated intravascular coagulation (DIC) were
emerged. The patient was retrieved to mechanical
ventilation with therapeutic and supportive interventions. Despite all measures she did not respond to
treatment and unfortunately died on the 10th day of
the chemotherapy.
This case was considered noteworthy to be
presented with its clinical presentation suggesting
complicated erysipelas that has leaded to a delay
in the diagnosis and a fatal outcome due to the aggressive clinical course.
Cases with primary cutaneous anaplastic large
cell lymphoma, particularly those with an initial presentation of extensive limb disease (ELD), defined
as multiple skin tumors in 1 limb or contiguous body
regions, have a more aggressive course and may
need a more aggressive treatment because of the
poorer outcomes.1,2
Figure 1. The erythematous, indurated soft tissue lesion
on the right thigh.
Blood cultures revealed no bacterial growth.
Patient did not respond to antibiotic therapy. Histopathology of the skin biopsy was consistent with
diffuse anaplastic large cell lymphoma. Hematology
consultation was conducted on the same day of the
pathology result and chemotherapy with CHOP (cy-
J Microbiol Infect Dis
REFERENCES
1. Woo DK, Jones CR, Vanoli-Storz MN, et al. Prognostic factors in primary cutaneous anaplastic large cell lymphoma:
characterization of clinical subset with worse outcome. Arch
Dermatol 2009; 145:667-674.
2. Diamantidis MD; Papadopoulos A; Kaiafa G, et al. Differential
diagnosis and treatment of primary, cutaneous, anaplastic
large cell lymphoma: not always an easy task. Int J Hematol
2009; 90:226-229.
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