Janie Bujold

Centre Intégré de Santé et Services Sociaux de la Gaspésie

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A case of relapsed systemic multiple myeloma mimicking adenopathy and extensive skin patch overlying a plasmacytoma

JAAD Case Reports (2022)

Valérie Tremblay-Abel Janie Bujold Bernard Delisle

Multiple myeloma rarely metastasizes to the skin and when it does, it usually manifests as cutaneous nodules. In this report, we describe a new clinical presentation of metastatic multiple myeloma mimicking AESOP syndrome in association with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes (POEMS) syndrome.

POEMS syndrome

Organomegaly

Monoclonal gammopathy

10.1016/j.jdcr.2022.05.019

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Eosinophilic Fasciitis Occurring under Treatment with Natalizumab for Multiple Sclerosis

Journal of Cutaneous Medicine and Surgery (2014)

Janie Bujold C. Boivin Mohamed Amin Jean‐Pierre Bouchard Jacques Soucy

Background: Eosinophilic fasciitis is a rare sclerosing syndrome with a poorly understood etiology. Objective: We report a case of eosinophilic fasciitis in a 40-year-old man undergoing treatment with natalizumab for multiple sclerosis. Natalizumab is a selective adhesion molecule inhibitor that prevents interaction of leukocytes with endothelial cells. Peripheral blood eosinophilia has been described under treatment with natalizumab, but we herein report the first case to our knowledge of eosinophilic fasciitis as a possible complication of this medication.

Natalizumab

Eosinophilic fasciitis

Etiology

10.2310/7750.2013.13026

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Citations (17)

A Rare Case of Oestrogen Dermatitis

Journal of Cutaneous Medicine and Surgery (2016)

Émilie Bourgeault Janie Bujold Marie-Ève Doucet

Background: Oestrogen dermatitis is a rare disorder characterised by cyclical eruptions in association with a woman’s menstrual cycle. Methods: A 43-year-old woman with an 8-year history of cyclical inguinal dermatitis, with a negative patch test, was tested with intradermal progesterone and oestrogen. Results: Intradermal testing was positive for oestrogen only. Conclusion: In a female patient with cyclical dermatitis, it is important to consider oestrogen or progesterone dermatitis in the differential diagnosis.

10.1177/1203475416685075

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A rare case of late myelodysplasia cutis associated with essential thrombocythemia: A case report

SAGE Open Medical Case Reports (2022)

Suzel Fournier Sylvain Mailhot Janie Bujold

Myelodysplasia cutis is a relatively new described entity that is characterized by cutaneous plaques and nodules representing dermal infiltration of myeloid immature non-blastic cells. It can be related to myelodysplastic syndromes or myeloproliferative disorders. It has distinct clinical and histopathological features in comparison with leukemia cutis. We report an unusual case of late myelodysplasia cutis in a male patient with essential thrombocythemia. It is only the second case reported to be related to this myeloproliferative disorder.

Leukemia cutis

Myeloproliferative Disorders

Cutis

Infiltration (HVAC)

Scarring alopecia

10.1177/2050313x221085760

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A Unique Case of Cutaneous Larva Migrans Acquired Within the Province of Quebec and Successfully Treated With Topical Ivermectin

Journal of Cutaneous Medicine and Surgery (2018)

Anne-Sophie Smilga Janie Bujold

Cutaneous larva migrans (CLM) is a zoonotic helminthiasis frequently imported to Canada by travellers to beach destinations in the tropics. The preferred treatment is oral ivermectin. We present a case of CLM acquired within the province of Quebec, a first in our provincial health records. Our case also puts forward the use of topical ivermectin as a possibly effective CLM treatment approach as our patient was successfully treated with 1 month of an ivermectin 1% cream applied locally twice daily.

Cutaneous larva migrans

10.1177/1203475418755763

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A Rare Case of Solitary Giant Congenital Juvenile Xanthogranuloma: A Case Report

Journal of Cutaneous Medicine and Surgery (2017)

Catherine Vignault Émilie Bourgeault Éric Gagné Janie Bujold

Juvenile xanthogranuloma (JXG) is the most frequent form of non–Langerhans cell histiocytosis. We present a case of giant congenital JXG in a 7-week-old boy, who had a firm and incompressible lesion, measuring 3 × 4 cm in diameter, on his right flank. The clinical appearance of the lesion and the ultrasound results suggested a vascular tumor, such as a hemangioma. Histology confirmed a JXG, although there was an absence of Touton cells, which are usually pathognomonic of JXG. In light of these findings, it would be important to include JXG in the differential diagnosis of congenital tumours, particularly vascular lesions.

Juvenile xanthogranuloma

10.1177/1203475417690718

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Citations (5)

Early disseminated cutaneous Lyme disease with SIADH, transaminitis, and pancytopenia: A case report

SAGE Open Medical Case Reports (2025)

Louis Deschênes Philippe Jutras Janie Bujold

Lyme disease is a tick-borne disease predominantly caused by Borrelia burgdorferi in Canada. Early disseminated disease is challenging to diagnose and requires treatment to prevent severe sequelae. We report the case of a 71-year-old woman who was admitted for a fever. Her blood tests showed a syndrome of antidiuretic hormone secretion, transaminitis, and pancytopenia. During hospitalization, the patient was noted to have an initial annular patch, which was followed by multiple diffuse erythematous patches. After a comprehensive medical history by a dermatology consultant highlighting an exposure to a tick bite, early disseminated disease was diagnosed, and a complete remission was obtained with Doxycycline. Dermatologists must maintain a high clinical suspicion for Lyme disease.

LYME

10.1177/2050313x251320186

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JAAD Case Reports Article List

Journal of the American Academy of Dermatology (2022)

Haiqing Wang Chao Ji Ting Gong Dirk M. Elston Celine Phong

10.1016/s0190-9622(22)02270-8

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