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Thank you for your interest in the ASDP Case Study of the Month. This form will allow you to submit your case easily. You will receive an email when your submission is complete confirming that we have received your case. If you do not receive that email confirmation within 24 hours, please email [email protected] and notify us. Please include the title of your case.

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Submitter

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Title

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Authors

You are limited to two authors. A third author can be included if they are a physician-in-training.

*Total Number of Authors:

-- 1 2 3

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Questions

*Total Number of Questions:

-- 1 2 3 4 5

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Conclusion or References

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*Conclusion/References:

Diagnosis

*Diagnosis:

Acquired Elastotic Hemangioma Acrodermatitis enteropathica ‎ African tick bite fever Aggressive Digital Adenocarcinoma Angioimmunoblastic T-cell lymphoma Angiokeratoma Angiomatoid Fibrous Histiocytoma Aprocrine Clear Cell Hidradenoma Basal cell carcinoma Basaloid follicular hamartoma Blastomycosis Bullous mastocytosis Calcifying Aponeurotic Fibroma Cellularneurothekeoma Clear cell acanthoma with changes of eccrine syringofibrodenoma Condyloma Lata Cranial Fasciitis Cutaneous lymphadenoma Cutaneous metaplastic synovial cyst Cutaneous Rosai-Dorfman Disease Cutaneous syncytial myoepithelioma Cystic panfolliculoma Eccrine Squamous Syringometaplasia Elastofibroma Endocrine Mucin Producing Carcinoma Endometriosis Eosinophilic pustular folliculitis of infancy Epidermal Panfolliculoma Epidermodysplasia Verruciformis Epidermolytic Hyperkeratosis Epithelial sheath neuroma Epithelioid Angiosarcoma Epithelioid Hemangioendothelioma Epithelioid hemangioma Epithelioid melanocytic tumor with BAP1 genomic loss Erythema elevatum diutinum Extra-axial chordoma Extramammary Fibroadenoma Fibroblastic connective tissue nevus Fibrous Hamartoma of Infancy Fibrous Papule Fusarium Moniliforme Giant cell angiofibroma Giant Cell Fibroblastoma Giant Cell Tumor (Tenosynovial, diffuse type) (DCGT) Glomeruloid hemangioma Glomus Tumor Granularcell Dermafibroma Infantile digital fibromatosis Infectious panniculitis Intralymphatic histiocytosis Intravascular large B-cell lymphoma Intravascularhistiocytosis Ischemic Fasciitis Juvenile hyaline fibromatosis Kaposi Sarcoma Leishmaniasis Leprosy Lichen amyloidosis Lichen striatus  Linear lgA Bullous Dermatosis Localized lipodystrophy ‎ Low Grade Fibromyxoid Sarcoma Lyme Disease Lymphoepithelioma-like carcinoma Lymphoplasmacytic Lymphoma Malignantmelanoma and basal cell carcinoma Mammary-type myofibroblastoma Mantle Cell Lymphoma Massive localized lymphedema (MLL) Metastatic adenocarcinoma of prostate Metastatic Chordoma Metastatic small cell lung carcinoma Microvenular Hemangioma Multinucleate Cell Angiohistiocytoma Mycobacterial Spindle Cell Pseudotumor Myoepithelioma Myofibroma Myxoinflammatory Fibroblastic Sarcoma Neurocristic Hamartoma Neurofollicular hamartoma Oncocytoma Onychomatricoma Ossifying fibromyxoid tumor Palisaded Neutrophilic Granulomatous Dermatitis Papular acantholytic dyskeratosis Paraneoplastic Pemphigus Pemphigus vegetans Phosphaturic Mesenchymal Tumor Pilomatrical carcinoma Pityriasis Rubra Pilaris Pleomorphic Hyalinizing Angiectatic Tumor Porocarcinoma Porokeratosis Ptychotropica Porphyria cutanea tarda Postoperative Alopecia Primary Cutaneous Perivascular Epithelioid Cell Primary syphilitic chancre Protothecosis Pseudomyogenic hemangioendothelioma Pseudoxanthoma elasticum-like papillary dermal elastosis Renal Cell Carcinoma Metastasis Reticular perineurioma Rosai-Dorfman Disease Rudimentary Meningocele Schnitzler syndrome Sclerodermoid graft-versus-host-disease Sclerotic dermatofibrosarcoma protuberans Signet ring cell carcinoma Sinusoidal Hemangioma Solitary adult myofibrom Superficial Acral Fibromyxoma Synovial Sarcoma Tattoo reaction T-cell Rich Angiomatoid Polypoid Psedulymphoma Telangiectasia macularis eruptiva perstans (TMEP) Trauma related to styling Trichogerminoma Verruciform Xanthoma Verrucous venous malformation Other

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*By submitting this case the author transfers, assigns, or otherwise conveys all copyright ownership of the case study to the American Society of Dermatopathology in the event the case study is published on the ASDP Web site. The author also warrants that the case study is original in form and substance, a case study of similar content has not been published in print or digital medium under my authorship, does not infringe on any copyright or other proprietary right of any third party, and is not under consideration by another publisher or journal.:

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