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A man had two rare autoimmune diseases that might be connected.

The man's hair loss and skin papules were diagnosed as atrichia with papular lesions, not alopecia areata universalis.

A woman with lupus also developed a severe skin condition linked to a genetic factor.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Polypoid cystitis can mimic bladder cancer but can be effectively treated with surgery, stents, and medication.

Combining medication and minimally invasive techniques can effectively manage Marine-Lenhart syndrome.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

The condition is likely inherited in an autosomal-dominant pattern.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

A woman had high testosterone due to an ovarian issue, which was fixed with surgery.

The report concludes that atypical Brauer nevus is more common in males, present at birth, and often misdiagnosed due to its unusual scalp locations.

Popliteal Artery Entrapment Syndrome (PAES) is a rare but possible cause of leg pain during walking, even in untrained women.

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

A woman had unusual hair growth on one side of her chin without a known cause.

A woman with skin and joint issues progressed from one type of lupus to another, highlighting the need to recognize complex conditions.

Trichoblastomas in rabbits are linked to uncontrolled embryonic hair growth and have distinct histological features.

A rare skin tumor with extra hair growth was found and safely removed from a 27-year-old woman.

Apocrine type cutaneous mixed tumors often resemble hair follicles, sebaceous glands, and apocrine glands.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

A 20-year-old woman had stable Progressive Hemifacial Atrophy and Vitiligo after treatment, suggesting a possible link between the conditions.

A rare ovarian cancer with a good outlook was found in a woman with unusual hair growth and abdominal symptoms.

A benign tumor on the cheek, called trichoadenoma, should be surgically removed for cosmetic reasons.

A woman with Degos disease managed her condition for nine years with medications and had two healthy pregnancies, while a separate finding suggests a possible link between female pattern hair loss and high blood pressure.

A specific gene mutation causes Olmsted syndrome.

MESTSV is a rare tumor that is mostly benign but needs long-term monitoring due to potential recurrence.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.