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1.
Cureus ; 15(10): e47953, 2023 Oct.
Article in English | MEDLINE | ID: mdl-38034254

ABSTRACT

Distant renal cell carcinoma (RCC) metastatic disease is mostly seen in the lungs, bones, and lymph nodes. The incidence of local recurrences within the ipsilateral retroperitoneum (RFR) is very low. We report a case of a 79-year-old male with recurrent left renal fossa RCC with pancreatic tail invasion who presented with large bowel obstruction. To the best of our knowledge, no cases have been reported of recurrent left renal fossa RCC initially presenting as extrinsic large bowel obstruction.

2.
Medicine (Baltimore) ; 102(41): e35622, 2023 Oct 13.
Article in English | MEDLINE | ID: mdl-37832062

ABSTRACT

RATIONALE: Septic thrombophlebitis of the internal jugular vein also known as Lemierre syndrome occurs secondary to an oropharyngeal infection often leading to septic embolisms to distant sites. Anaerobic gram-negative bacillus, Fusobacterium nucleatum and Fusobacterium necrophorum are commonly isolated organisms. Fusobacterium species has also been reported to complicate an intra-abdominal infection leading to septic thrombophlebitis of portal vein also known as pylephlebitis or abdominal variant of lemierre syndrome. PATIENT CONCERNS: The patient was a middle-aged female patient with chief complaints of abdominal discomfort, intermittent fever and vomiting for one month. DIAGNOSES: The final diagnosis was septic thrombophlebitis of portal and splenic vein secondary to Fusobacterium nucleatum. INTERVENTIONS: Patient was managed with broad spectrum intravenous antibiotics with coverage against gram-negative bacilli, anaerobes, and aerobic streptococcus species with therapeutic anticoagulation. OUTCOMES: Patient gradually improved and was discharged on oral apixaban. She was instructed to follow up with gastrointestinal specialist upon discharge in anticipation of the need for liver transplant in future. LESSONS: Due to its high mortality and associated long term disease morbidity, clinicians should always strive towards early diagnosis and treatment of the condition with involvement of multidisciplinary teams.


Subject(s)
Lemierre Syndrome , Soft Tissue Infections , Thrombophlebitis , Middle Aged , Humans , Female , Lemierre Syndrome/complications , Lemierre Syndrome/diagnosis , Lemierre Syndrome/drug therapy , Fusobacterium nucleatum , Splenic Vein , Thrombophlebitis/etiology , Abdomen , Jugular Veins
3.
Pan Afr Med J ; 45: 141, 2023.
Article in English | MEDLINE | ID: mdl-37808429

ABSTRACT

Acral lentiginous melanoma (ALM) is a type of melanoma that is traditionally seen on the soles of the feet, palms of the hand, and under the fingernails or toenails. It is the least frequently diagnosed melanoma among the four histologic subtypes of cutaneous melanoma, accounting for less than 5% of all cases. ALM is frequently diagnosed at late stages and has higher incidences in non-white populations in relation to the other forms of cutaneous malignant melanoma. The most common sites of metastases in melanoma are the skin and subcutaneous tissue followed by lung, liver, brain, and bone. Bone metastases from malignant melanoma usually occur in patients who already have widespread metastases. We present this paper as a unique case study of ALM lesion in an 84-year-old African American male presenting originally in the base of right fifth toe plantar aspect then found multiple bone metastases without any other organ involved.


Subject(s)
Bone Neoplasms , Melanoma , Skin Neoplasms , Humans , Male , Aged, 80 and over , Melanoma/pathology , Skin Neoplasms/pathology , Skin/pathology , Foot/pathology , Bone Neoplasms/diagnosis , Bone Neoplasms/pathology , Melanoma, Cutaneous Malignant
4.
J Investig Med High Impact Case Rep ; 10: 23247096211060581, 2022.
Article in English | MEDLINE | ID: mdl-35277086

ABSTRACT

Antiphospholipid syndrome (APS) may be either as a primary or in association with an underlying systemic autoimmune etiology (36.2%), particularly systemic lupus erythematosus (SLE). Thrombocytopenia is infrequently observed in APS patients, with an occurrence of 22% to 42% with the frequency of thrombocytopenia, higher in APS and SLE combination than in primary APS. There have been some controversial reports regarding the treatment of APS syndrome with thrombocytopenia with TPO agonists. We like to report a case with APS syndrome with severe thrombocytopenia treated with TPO-RA and developed severe thrombocytosis and thrombosis. Our case represented the first case of TPO-RA in treating APS syndrome developed severe thrombocytosis and our case also concurred that use of TPO-RA agents should be strongly discouraged in APS until larger studies clarify the safety of TPO-RA agents in APS.


Subject(s)
Antiphospholipid Syndrome , Lupus Erythematosus, Systemic , Purpura, Thrombocytopenic, Idiopathic , Thrombocytopenia , Thrombocytosis , Thrombosis , Antiphospholipid Syndrome/complications , Antiphospholipid Syndrome/drug therapy , Benzoates , Humans , Hydrazines , Lupus Erythematosus, Systemic/complications , Purpura, Thrombocytopenic, Idiopathic/chemically induced , Purpura, Thrombocytopenic, Idiopathic/complications , Purpura, Thrombocytopenic, Idiopathic/drug therapy , Pyrazoles , Thrombocytopenia/chemically induced , Thrombocytopenia/complications , Thrombocytosis/chemically induced , Thrombocytosis/complications , Thrombosis/chemically induced
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