Focal acantholytic dyskeratosis has a distinctive histological pattern that is associated with various clinical expressions. It rarely occurs on the lip or the perianal area. We report a patient with focal acantholytic dyskeratosis occurring on both the upper lip and the anal canal. Histopathologically, the lesions showed hyperkeratosis, suprabasilar clefting, epidermal acantholysis and dyskeratosis. This case represents the first report of a focal acantholytic dyskeratosis occurring on both the lip and the anal canal.
Acantholysis/*pathology ; Adult ; Anus Diseases/*pathology ; Human ; Keratosis/*pathology ; Lip Diseases/*pathology ; Male

OBJECTIVETo improve the recognization and treatment for oral venous lakes (OVL).

METHODSClinicopathologically analysis of 20 cases of oral venous lakes was performed. All the samples were removed by surgically.

RESULTSAll the lesions occurred in senile persons and located under the mucosa. Among the 20 cases, 11 were male patients and 9 were female; 18 of 20 occurred in the lower lip, another two in the upper lip and buccal mucosa. The lesions were 0.3 approximately 1.2 cm in size. Pathologically, the oral venous lake was composed of single or a few large, dilated and irregular veins. Thrombosis and organization were found within the lesions sometimes.

CONCLUSIONSOral venous lakes are a kind of focal anomalies of venous structure. All the 20 cases (with a follow-up time from 8 months to 4 years) has no recurrence after surgical treatment.

Aged ; Diagnosis, Differential ; Female ; Humans ; Lip Diseases ; diagnosis ; pathology ; surgery ; Male ; Middle Aged ; Mouth Mucosa ; pathology ; Vascular Diseases ; pathology ; surgery

Laugier-Hunziker syndrome (LHS) is an acquired pigmentary condition affecting lips, oral mucosa and acral area, frequently associated with longitudinal melanonychia. There is neither malignant predisposition nor underlying systemic abnormality associated with LHS. Herein, we present three uncommon cases of LHS with possibly new feature of nail pigmentation, which were diagnosed during the past 2 years. We also review the clinical and histological findings, differential diagnosis, and treatment of the syndrome in published literature.
Adult ; Female ; Gingival Diseases ; diagnosis ; Humans ; Hyperpigmentation ; diagnosis ; Lip Diseases ; diagnosis ; Male ; Melanins ; analysis ; Middle Aged ; Mouth Diseases ; diagnosis ; Mouth Mucosa ; pathology ; Nail Diseases ; diagnosis ; Syndrome ; Tongue Diseases ; diagnosis

We report a 59-year-old patient with malignant acanthosis nigricans associated with metastasis of endometrial carcinoma. The patient presented papillomatosis lesions that appeared to be benign on multiple skins of body folds, particularly on lips. The lesions in lips and axilla had histological characteristic appearances of acanthosis nigricans, while the masses in abdomen and pelvis were metastasis endometrial adenocarcinoma. The article highlights the importance of biopsy and histopathological diagnosis in presumed benign lesions and the role of doctors in screening for body internal tumors.
Abdominal Neoplasms ; secondary ; Acanthosis Nigricans ; pathology ; Adenocarcinoma ; secondary ; Endometrial Neoplasms ; pathology ; Female ; Follow-Up Studies ; Humans ; Lip Diseases ; pathology ; Lymphatic Metastasis ; pathology ; Middle Aged ; Paraneoplastic Syndromes ; pathology ; Pelvic Neoplasms ; secondary

Lymphocytic interstitial pneumonia(LIP) is an uncommon condition in which the alveolar septa and extra-alveolar interstitial space are markedly expanded by small lymphocytes, plasma cells and histiocytes. Chest radiographs generally show nonspecific patterns with the most common pattern showing bibasilar reticular or reticulonodular infiltrates. Hilar or mediastinal lymphadenopathy and pleural effusions are usually absent. We encountered a 42-year-old female patient who was admitted to hospital because of exertional dyspnea and palpitation. The chest X-ray showed an enlarged bilateral hilar shadow and diffusely increased bronchovascular markings in both lung fields. The chest CT showed diffuse nodular infiltrations with mild septal thickening and combined patchy ground glass opacity in both lungs, and conglomerated mediastinal and bilateral hilar lymphadenopathy. A diagnosis of LIP was made from the tissue pathology taken by a thoracoscopic lung biopsy. The patient showed clinical and radiographic improvement after 3 months of treatment with prednisolone. We report a case of LIP presenting as diffuse nodular interstitial infiltrations with multiple mediastinal and bilateral hilar lymphadenopathy.
Adult ; Biopsy ; Diagnosis ; Dyspnea ; Female ; Glass ; Histiocytes ; Humans ; Lip ; Lung ; Lymphatic Diseases* ; Lymphocytes ; Pathology ; Plasma Cells ; Pleural Effusion ; Prednisolone ; Radiography, Thoracic ; Thorax ; Tomography, X-Ray Computed