Histiocytoid Sweet syndrome may indicate leukemia cutis: A novel application of fluorescence in situ hybridization

• Published in: Journal of the American Academy of Dermatology 2014-06, Vol.70 (6), p.1021-1027
• Main Authors: Chavan, Rahul N., MD, PhD, Cappel, Mark A., MD, Ketterling, Rhett P., MD, Wada, David A., MD, Rochet, Nicole M., MD, Knudson, Ryan, BA, MBA, Gibson, Lawrence E., MD
• Format: Article
• Language: English
• Subjects: Aged; Aged, 80 and over; Biopsy, Needle; Chromosome Aberrations; Cohort Studies; Comorbidity; cytogenetic abnormalities; Dermatology; Female; fluorescence in situ hybridization analysis; Follow-Up Studies; Histiocytes - pathology; histiocytoid Sweet syndrome; Humans; Immunohistochemistry; In Situ Hybridization, Fluorescence - methods; Incidence; Leukemia - diagnosis; Leukemia - epidemiology; leukemia cutis; Male; malignancy-associated Sweet syndrome; Middle Aged; Retrospective Studies; Risk Assessment; Skin Neoplasms - diagnosis; Skin Neoplasms - epidemiology; Sweet syndrome; Sweet Syndrome - diagnosis; Sweet Syndrome - epidemiology
• ISSN: 0190-9622; 1097-6787
• DOI: 10.1016/j.jaad.2014.01.874

Background In patients with malignancy-associated Sweet syndrome, a thorough evaluation for leukemia cutis should be considered. Objective We sought to describe the clinicopathologic characteristics of histiocytoid Sweet syndrome. Methods We retrospectively identified patients with histiocytoid Sweet syndrome at our institution from January 1992 through December 2010. We evaluated the underlying cutaneous infiltrate using immunohistochemistry and fluorescence in situ hybridization. Results We re-evaluated all 22 patients with hematologic malignancy–associated Sweet syndrome. Six patients had a monocytoid infiltrate that was consistent with histiocytoid Sweet syndrome; subsequent evaluation of these patients demonstrated cytogenetic abnormalities on prior bone-marrow biopsy specimens. Fluorescence in situ hybridization analysis was feasible in cutaneous specimens from 5 of the 6 patients and demonstrated the same cytogenetic abnormalities that were identified on prior bone-marrow biopsy specimens in 4 patients. Therefore, these 4 patients may have had a form of leukemia cutis. Limitations This was a retrospective study. Conclusion For patients with histiocytoid Sweet syndrome, an underlying hematologic malignancy, and a monocytoid infiltrate on biopsy specimen, fluorescence in situ hybridization of the cutaneous infiltrate may be beneficial to identify cytogenetic abnormalities that may indicate leukemia cutis.