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1.
S D Med ; 77(4): 152-156, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38991158

ABSTRACT

Extramammary Paget's disease (EMPD) is an uncommon cutaneous neoplasm almost exclusively located in the vulvar, perianal, and male genitalia regions. Evaluation and management are complicated given the average delay in diagnosis is two years and approximately 30% of cases are associated with underlying malignancies. The axilla is a unique location for EMPD. We report a rare case of a 78-year-old male with axillary EMPD associated with an underlying adenocarcinoma. A 1-cm tender and pruritic erythematous plaque with surrounding erythema appeared in the patient's axilla. An irritated seborrheic keratosis secondarily impetiginized along with irritant contact dermatitis was suspected. Treatment of cefdinir and topical hydrocortisone failed and a biopsy was taken. Microscopic and immunohistochemical examination showed ulceration with an underlying proliferation of atypical glands (Figure 2A) and a nested intraepidermal proliferation with pagetoid spread (Figure 2B). The atypical cells were positive for gross cystic disease fluid protein 15 (Figure 2C), epithelial membrane antigen (Figure 2D), cytokeratin 5/6, and cytokeratin 7. These findings were supportive of an apocrine adenocarcinoma arising in association with EMPD. Wide location excision was performed. Screening for associated malignancies or lymphatic spread is the primary goal during evaluation. Outcomes are favorable when the primary neoplasm is of limited distribution. The accepted treatment for primary lesions is wide local excision, although anatomic tissue constraints necessitate further research into other treatment modalities. To our knowledge, this is the 14th reported case of axillary EMPD with an underlying adenocarcinoma which may help with identification and management of future cases.


Subject(s)
Adenocarcinoma , Axilla , Paget Disease, Extramammary , Humans , Paget Disease, Extramammary/diagnosis , Paget Disease, Extramammary/pathology , Aged , Male , Adenocarcinoma/pathology , Adenocarcinoma/diagnosis , Sweat Gland Neoplasms/pathology , Sweat Gland Neoplasms/diagnosis , Skin Neoplasms/pathology , Skin Neoplasms/diagnosis
2.
S D Med ; 77(1): 37-41, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38986147

ABSTRACT

Glomus tumors are rare vascular hamartomas most commonly found in the subungual region of the fingers. They present with a classic triad of paroxysmal pain, point tenderness, and cold sensitivity. The diagnosis is often missed for several years due to under recognition of this condition. A 42-year-old female presented with a several year history of pain in the middle finger when it was struck or exposed to cold. She had point tenderness on the fingernail, and increased curvature of the nail. Magnetic Resonance Imaging (MRI) revealed a 7mm subungual glomus tumor. The tumor was surgically excised via a transungual approach, resulting in complete relief of her pain. Glomus tumors are diagnosed clinically based on the presence of classic symptoms and positive provocative tests. These tests include point tenderness on palpation and pain when ice is placed on the digit. MRI imaging can be used when the diagnosis is unclear or to localize the tumor prior to surgery. Increased awareness of this condition among physicians could reduce the time to diagnosis and treatment.


Subject(s)
Fingers , Glomus Tumor , Magnetic Resonance Imaging , Humans , Glomus Tumor/diagnosis , Glomus Tumor/complications , Glomus Tumor/surgery , Female , Adult , Magnetic Resonance Imaging/methods , Pain/etiology , Pain/diagnosis , Nail Diseases/diagnosis , Nail Diseases/surgery , Nail Diseases/diagnostic imaging , Nail Diseases/etiology
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