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A special blood test helped find the overactive ovary in a teen with PCOS, and removing that ovary improved her condition.

A young man was unexpectedly diagnosed with basal cell carcinoma after a scalp examination and confocal microscopy.

A rare benign skin growth called melanocytic matricoma was identified in a 69-year-old man.

A woman's severe male hormone excess was caused by a small, hard-to-find ovarian tumor.

A young girl's foot lesion was actually a rare condition caused by a hair fragment under the skin, not a parasite.

Accurate diagnosis of Winer's dilated pore in the ear is crucial to avoid unnecessary aggressive treatment.

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

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

A 10-year-old boy recovered from a scalp infection caused by a fungus after treatment with itraconazole.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

A 36-year-old man had unusual skin lesions on his face without hair loss.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The boy's hair and skin color differences are due to a pigmentation disorder.

Accurate diagnosis of RDEB-mitis in older adults is crucial for proper management without immunosuppressants.

The case suggests that dissecting cellulitis of the scalp can occur in a White child and should be considered when diagnosing pediatric scarring alopecia.

A rare skin condition in children can look like other diseases.

Adenolipomas may develop from gland entrapment by fat tissue, showing complex and varied forms.

Congenital adrenal hyperplasia may be linked to adrenal myelolipoma.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A man with a skin nodule was diagnosed with a rare skin condition called cutaneous focal mucinosis, which can be confused with other skin cancers.

Multiple pilomatrixoma may indicate Turner syndrome.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

The junction of the inner and outer prepuce with good blood flow is best for vascular pedicle flaps.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.

Tiny infundibular cysts are the main lesions in chloracne, not comedones.

Radiation cystitis patients need better monitoring and early treatment due to higher readmission rates.

A rare ovarian tumor can cause unusual male-like symptoms, but surgery usually leads to a good outcome.

A 25-year-old man had an unusual case of benign skin tumors and hair loss.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

A rare skin condition causes red and dark patches on the face and limbs.