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Post-scabietic nodules: Mimicker of infantile indeterminate cell histiocytosis and potential diagnostic pitfall
Kristen N Ruby1, Eric Y Loo1, Julianne A Mann2
1Department of Pathology and Laboratory Medicine, Geisel School of Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Insights
Indeterminate cell histiocytosis (ICH) is a rare skin condition. Post-scabetic nodules can mimic ICH, highlighting the importance of clinical context for accurate diagnosis and treatment.
Area of Science:
- Dermatology
- Histopathology
- Pediatrics
Background:
- Indeterminate cell histiocytosis (ICH) is an exceptionally rare disorder with unknown etiology.
- Patients typically exhibit dermal nodules composed of indeterminate cells, resembling Langerhans cells but lacking Birbeck granules.
- The clinical presentation of ICH is variable, with outcomes ranging from spontaneous resolution to aggressive disease progression.
Observation:
- Rare instances of ICH-like reactions have been documented following scabies infestations and arthropod bites (ticks, mosquitos).
- This report details a successfully treated case of indeterminate cell-rich post-scabetic nodules in an 8-month-old boy.
- The lesions mimicked ICH but were associated with a prior scabies infestation.
Findings:
- Histopathological examination revealed nodules rich in indeterminate cells.
- The patient, an otherwise healthy infant, showed a positive response to treatment.
- Literature review identified similar ICH-mimicking lesions in the context of scabies.
Implications:
- Accurate interpretation of ICH-mimicking lesions requires careful consideration of the clinical context, particularly in cases of scabies.
- Distinguishing these indolent lesions from true ICH is crucial to avoid unnecessary patient anxiety and overly aggressive treatment strategies.
- This case underscores the importance of a comprehensive diagnostic approach in pediatric dermatology.
Abstract:
Indeterminate cell histiocytosis (ICH) is an extremely rare disease and little is known about its etiology. Patients usually present with nodular, dermal proliferations of indeterminate cells, which characteristically resemble Langerhans cells but lack Birbeck granules. The clinical course is highly variable, ranging from spontaneous regression to rapid progression with reports of extracutaneous involvement, subsequent acute myeloid leukemias, and associated B-cell lymphomas. Rare cases of ICH-like reactions have been reported in the setting of scabies infestations as well as in patients who had been bitten by ticks and mosquitos. We present a successfully treated case of indeterminate cell-rich post scabietic nodules in an otherwise healthy 8-month-old boy and review the literature on similar cases. Clinical context is essential for correct interpretation of these indolent ICH-mimicking lesions, and to avert unnecessary patient anxiety and aggressive management.
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