Abstract: RAS-associated autoimmune leukoproliferative disease (RALD) is a recently described noninfectious and nonmalignant clinical syndrome characterized by autoimmune disorders, massive splenomegaly, modest lymphadenopathy, and monocytosis. On the molecular level, RALD is defined by somatic mutations of either NRAS or KRAS gene in a subset of hematopoietic cells. To date, there is a dearth of well-documented histopathologic description of cutaneous involvement by RALD in the literature. In the current case report, a 43-year-old female patient with a history of RALD presented with clinical pictures of sepsis and an erythematous rash in the left lower extremity. Histologic examination revealed a dense perivascular and interstitial infiltrate of immature myeloid cells admixed with scattered neutrophils involving the dermis and subcutaneous adipose tissue, imparting a panniculitis-like histologic pictures. There was a strong angiocentric propensity of the immature hematopoietic cells as well as extensive extravasation of red blood cells, even in the subcutaneous adipose tissue. Immunohistochemically, the immature hematopoietic cells were positive for CD43, CD4, and CD68, but negative for CD34, CD117, and myeloperoxidase. Overall, the histologic and cytologic findings were highly reminiscent of histiocytoid Sweet syndrome. Review of the English literature revealed cutaneous involvements by RALD only in patients with KRAS mutation compared with none of its NRAS counterparts. However, larger clinicopathologic studies on cutaneous involvement by RALD are warranted. The term "RALD cutis" with its histologic and molecular features is suggested to serve as a potential groundwork for future studies of this rare phenomenon. Correspondence: Tien Anh N. Tran, MD, Department of Pathology, Florida Hospital Orlando, 601 East Rollins Street, Orlando, FL 32803 (e-mail: tien.tran.md@flhosp.org). The authors declare no conflicts of interest. Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved.
http://bit.ly/2Q7B33S
Σφακιανάκης Αλέξανδρος
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5 Άγιος Νικόλαος
Κρήτη 72100
00302841026182
00306932607174
alsfakia@gmail.com
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- Moving forward with improved food labelling for co...
- Forthcoming Meetings
- Best of the Other Journals
- Anthony J Frew
- Issue Information
- Editorial
- Intravenously administered cloxacillin-induced neu...
- Syndrome POEMS
- TIMP-3 suppression induces choroidal neovasculariz...
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- Right hemisphere superiority for executive control...
- 18F-choline PET/CT incidental thyroid uptake in pa...
- 18F-choline PET/CT incidental thyroid uptake in pa...
- Modiolar rotational cheiloplasty: Addressing the c...
- Carcinoma Presenting as Idiopathic Anterior Glotti...
- The presence of eosinophil aggregates correlates w...
- Cervical slide tracheoplasty in adults with laryng...
- Efficacy of tranexamic acid on operative bleeding ...
- Comparison of endoscopic and microscopic ear surge...
- Septal fractures predict poor outcomes after close...
- Contemporary Review and Case Report of Botulinum R...
- Otosyphilis: Resurgence of an Old Disease
- The Socioeconomics of Atopic Dermatitis
- Early detection of esophageal second primary tumor...
- Comparison of contemporary staging systems for oro...
- Impact of social deprivation on the outcome of maj...
- Long‐term outcome and pattern of failure for patie...
- Polyethylene Glycol fusion associated with anti‐ox...
- Issue Information
- Surgical anatomy of the parapharyngeal space: A mu...
- Secretory carcinoma of the major salivary gland: A...
- Ichthyosiform sarcoidosis: a mimic of leprosy?
- Lupus erythematosus profundus in a patient with de...
- Sex‐related differences of clinical features in hi...
- Tuberculides and extrapulmonary TB: an atypical ma...
- A semiquantitative grading scale for frontal and v...
- Occupational human infestation due to “Martin bug”...
- Ichthyosiform sarcoidosis: a mimic of leprosy?
- Expansion of FOXP3+ regulatory CD4 T‐cells upon ex...
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